{
  "version": "https://jsonfeed.org/version/1.1",
  "title": "Recall Radar latest recalls",
  "home_page_url": "https://notyetneeded.com/latest-recalls",
  "feed_url": "https://notyetneeded.com/feed.json",
  "description": "Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.",
  "language": "en-US",
  "authors": [
    {
      "name": "Not Yet Needed"
    }
  ],
  "items": [
    {
      "id": "Drugs-99837-20260916",
      "url": "https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22",
      "title": "Drugs: fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City L...",
      "content_text": "Not Yet Classified Ongoing\nFirm: OurPharma LLC\nReason: Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).\nDistribution: Nationwide within the U.S\nRecall began: 2026-09-03\nFDA IDs:  / event 99837\nSource: https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Not Yet Classified",
        "Ongoing"
      ]
    },
    {
      "id": "D-0836-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22",
      "title": "Drugs: Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewat...",
      "content_text": "Class III Ongoing\nFirm: Ajanta Pharma USA Inc\nReason: Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.\nDistribution: Nationwide within the U.S\nRecall began: 2026-08-25\nFDA IDs: D-0836-2026 / event 99733\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "D-0835-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22",
      "title": "Drugs: Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprim...",
      "content_text": "Class III Ongoing\nFirm: ImprimisRx NJ LLC\nReason: Subpotent Drug\nDistribution: USA Nationwide\nRecall began: 2026-08-24\nFDA IDs: D-0835-2026 / event 99756\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "H-1341-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22",
      "title": "Food: Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506",
      "content_text": "Class I Ongoing\nFirm: International Sprout Holdings, Inc\nReason: Potential E. coli and Salmonella contamination\nDistribution: Wholesale consignees in 16 states: CA, FL, HI, IL, MA, MN, MO, MT, NY, OH, OR, PA, TN, SC, TX, UT; Puerto Rico; Canada, Mexico, Tahiti, and Venezuela\nRecall began: 2026-08-23\nFDA IDs: H-1341-2026 / event 99822\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Food",
        "Class I",
        "Ongoing"
      ]
    },
    {
      "id": "D-0850-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22",
      "title": "Drugs: Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, N...",
      "content_text": "Class I Ongoing\nFirm: Baxter Healthcare Corporation\nReason: Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.\nDistribution: U.S. Nationwide.\nRecall began: 2026-08-17\nFDA IDs: D-0850-2026 / event 99679\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class I",
        "Ongoing"
      ]
    },
    {
      "id": "H-1334-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22",
      "title": "Food: Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz",
      "content_text": "Class II Ongoing\nFirm: Ferrero USA\nReason: Undeclared milk and pecans\nDistribution: IA, IL, IN, OH\nRecall began: 2026-08-14\nFDA IDs: H-1334-2026 / event 99682\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Food",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "H-1330-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22",
      "title": "Food: Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients: B...",
      "content_text": "Class I Ongoing\nFirm: EXOTIQUE FOODS CANADA\nReason: Undeclared Wheat.\nDistribution: Product was sold in the U.S.\nRecall began: 2026-08-07\nFDA IDs: H-1330-2026 / event 99636\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Food",
        "Class I",
        "Ongoing"
      ]
    },
    {
      "id": "H-1335-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22",
      "title": "Food: Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold...",
      "content_text": "Class II Ongoing\nFirm: L-Nutra Inc\nReason: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.\nDistribution: Product is sold exclusively from the recalling firm's online website nationwide.\nRecall began: 2026-08-07\nFDA IDs: H-1335-2026 / event 99675\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Food",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3111-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22",
      "title": "Devices: Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR...",
      "content_text": "Class II Ongoing\nFirm: Atrium Medical Corporation\nReason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.\nDistribution: US Nationwide distribution.\nRecall began: 2026-08-07\nFDA IDs: Z-3111-2026 / event 99680\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3113-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22",
      "title": "Devices: Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);",
      "content_text": "Class II Ongoing\nFirm: Atrium Medical Corporation\nReason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.\nDistribution: US Nationwide distribution.\nRecall began: 2026-08-07\nFDA IDs: Z-3113-2026 / event 99680\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3110-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22",
      "title": "Devices: Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at...",
      "content_text": "Class II Ongoing\nFirm: Lutronic Corporation\nReason: Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.\nDistribution: Worldwide distribution - US Nationwide and the countries of Canada and European Union.\nRecall began: 2026-08-06\nFDA IDs: Z-3110-2026 / event 99601\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3133-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22",
      "title": "Devices: MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201",
      "content_text": "Class II Ongoing\nFirm: Nipro Renal Soultions USA, Corporation\nReason: Hemodialysis concentrates contain high endotoxin levels\nDistribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.\nRecall began: 2026-08-05\nFDA IDs: Z-3133-2026 / event 99573\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3134-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22",
      "title": "Devices: MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))",
      "content_text": "Class II Ongoing\nFirm: Nipro Renal Soultions USA, Corporation\nReason: Hemodialysis concentrates contain high endotoxin levels\nDistribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.\nRecall began: 2026-08-05\nFDA IDs: Z-3134-2026 / event 99573\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3136-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22",
      "title": "Devices: Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)",
      "content_text": "Class II Ongoing\nFirm: Nipro Renal Soultions USA, Corporation\nReason: Hemodialysis concentrates contain high endotoxin levels\nDistribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.\nRecall began: 2026-08-05\nFDA IDs: Z-3136-2026 / event 99573\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "H-1331-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22",
      "title": "Food: Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen",
      "content_text": "Class I Ongoing\nFirm: EURO FOODS GROUP USA NJ INC\nReason: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.\nDistribution: The adulterated product was distributed to the following states: VA, NY, NJ, MI\nRecall began: 2026-08-01\nFDA IDs: H-1331-2026 / event 99684\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Food",
        "Class I",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3138-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22",
      "title": "Devices: AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B",
      "content_text": "Class II Ongoing\nFirm: Windstone Medical Packaging, Inc.\nReason: The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.\nDistribution: US Nationwide distribution in the states of CA, GA, WA.\nRecall began: 2026-07-29\nFDA IDs: Z-3138-2026 / event 99658\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3120-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22",
      "title": "Devices: HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (Americ...",
      "content_text": "Class II Ongoing\nFirm: HeartSine Technologies Ltd\nReason: Due to a damaged (over stretched) membrane tail that causes an intermittent fault.\nDistribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME MI, MN, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SD,TN, TX, UT, VA, WA, WI, WV and WY. The countries of Argentina, Australia,...\nRecall began: 2026-07-27\nFDA IDs: Z-3120-2026 / event 99568\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3114-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22",
      "title": "Devices: Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 0080...",
      "content_text": "Class II Ongoing\nFirm: C.R. Bard Inc\nReason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.\nDistribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...\nRecall began: 2026-06-25\nFDA IDs: Z-3114-2026 / event 98840\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3115-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22",
      "title": "Devices: Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 94731...",
      "content_text": "Class II Ongoing\nFirm: C.R. Bard Inc\nReason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.\nDistribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...\nRecall began: 2026-06-25\nFDA IDs: Z-3115-2026 / event 98840\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3118-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22",
      "title": "Devices: Products that contain the Pericare Wipes: SureStep\" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 008017...",
      "content_text": "Class II Ongoing\nFirm: C.R. Bard Inc\nReason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.\nDistribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...\nRecall began: 2026-06-25\nFDA IDs: Z-3118-2026 / event 98840\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "Z-3119-2026",
      "url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22",
      "external_url": "https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22",
      "title": "Devices: Products that contain the Pericare Wipes: (Canada Only) SureStep\" Foley Tray System Bardex¿ IC Complete Care¿ REF: A3003...",
      "content_text": "Class II Ongoing\nFirm: C.R. Bard Inc\nReason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.\nDistribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and W...\nRecall began: 2026-06-25\nFDA IDs: Z-3119-2026 / event 98840\nSource: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22",
      "date_published": "2026-09-16T00:00:00.000Z",
      "tags": [
        "Devices",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0833-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22",
      "title": "Drugs: Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solut...",
      "content_text": "Class III Ongoing\nFirm: Supernus Pharmaceuticals, Inc.\nReason: Failed dissolution specifications.\nDistribution: US Nationwide.\nRecall began: 2026-08-31\nFDA IDs: D-0833-2026 / event 99767\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "D-0834-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22",
      "title": "Drugs: traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zag...",
      "content_text": "Class II Ongoing\nFirm: Teva Pharmaceuticals USA, Inc\nReason: Presence of Foreign Tablets/Capsules\nDistribution: U.S. Nationwide\nRecall began: 2026-08-24\nFDA IDs: D-0834-2026 / event 99734\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0840-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22",
      "title": "Drugs: Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, C...",
      "content_text": "Class III Ongoing\nFirm: American Health Packaging\nReason: Labeling: Label Mix-up\nDistribution: US Nationwide.\nRecall began: 2026-08-19\nFDA IDs: D-0840-2026 / event 99674\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "H-1304-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22",
      "title": "Food: Prince ITALIAN BREAD; Sesame; NET WEIGHT 8 OZ. (227g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FL...",
      "content_text": "Class III Ongoing\nFirm: Prince Bakery Inc\nReason: Sesame is not declared in the ingredient statement but is declared in the statement of identity.\nDistribution: New York.\nRecall began: 2026-08-13\nFDA IDs: H-1304-2026 / event 99646\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "H-1305-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22",
      "title": "Food: Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED FL...",
      "content_text": "Class III Ongoing\nFirm: Prince Bakery Inc\nReason: Sesame is not declared in the ingredient statement but is declared in the statement of identity.\nDistribution: New York.\nRecall began: 2026-08-13\nFDA IDs: H-1305-2026 / event 99646\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "D-0811-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22",
      "title": "Drugs: Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only...",
      "content_text": "Class II Ongoing\nFirm: Baxter Healthcare Corporation\nReason: CGMP Deviations\nDistribution: US Nationwide; Puerto Rico; and Chile.\nRecall began: 2026-08-06\nFDA IDs: D-0811-2026 / event 99500\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0813-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22",
      "title": "Drugs: CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/mL) in GALAXY Single-...",
      "content_text": "Class II Ongoing\nFirm: Baxter Healthcare Corporation\nReason: CGMP Deviations\nDistribution: US Nationwide; Puerto Rico; and Chile.\nRecall began: 2026-08-06\nFDA IDs: D-0813-2026 / event 99500\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0815-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22",
      "title": "Drugs: Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, St...",
      "content_text": "Class II Ongoing\nFirm: Baxter Healthcare Corporation\nReason: CGMP Deviations\nDistribution: US Nationwide; Puerto Rico; and Chile.\nRecall began: 2026-08-06\nFDA IDs: D-0815-2026 / event 99500\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0821-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22",
      "title": "Drugs: Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Co...",
      "content_text": "Class II Ongoing\nFirm: Baxter Healthcare Corporation\nReason: CGMP Deviations\nDistribution: US Nationwide; Puerto Rico; and Chile.\nRecall began: 2026-08-06\nFDA IDs: D-0821-2026 / event 99500\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "H-1308-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22",
      "title": "Food: Weis (Fresh From the Orchard ) Pasteurized Apple Cider, Contains 100 % Juice, the product comes in the following sizes:...",
      "content_text": "Class II Ongoing\nFirm: WEIS MARKETS, INC.\nReason: Product has high patulin levels\nDistribution: The recalled product was distributed to the State of PA.\nRecall began: 2026-08-06\nFDA IDs: H-1308-2026 / event 99638\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "D-0851-2026",
      "url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22",
      "external_url": "https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22",
      "title": "Drugs: Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & st...",
      "content_text": "Class I Ongoing\nFirm: OPTIMAL BALANCE PHARMACY\nReason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.\nDistribution: USA Nationwide.\nRecall began: 2026-08-05\nFDA IDs: D-0851-2026 / event 99662\nSource: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Drugs",
        "Class I",
        "Ongoing"
      ]
    },
    {
      "id": "H-1327-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22",
      "title": "Food: Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Homestyle Foods, LLC Richmond, V...",
      "content_text": "Class II Ongoing\nFirm: Ukrop's Homestyle Foods LLC\nReason: Foreign object: metal fragments\nDistribution: Product was shipped to the following states: KY, NC, VA & WVA.\nRecall began: 2026-07-30\nFDA IDs: H-1327-2026 / event 99548\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class II",
        "Ongoing"
      ]
    },
    {
      "id": "H-1320-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22",
      "title": "Food: Wonton Specialist Inc. Pan Fried Noodle, 16 oz and 5lb packaged in clear plastic bags",
      "content_text": "Class III Ongoing\nFirm: Wonton Specialists\nReason: Undeclared FD&C Red No. 40\nDistribution: NY, NJ, PA\nRecall began: 2026-07-28\nFDA IDs: H-1320-2026 / event 99508\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "H-1325-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22",
      "title": "Food: Wonton Specialist Inc. Cooked Noodle, 16 oz and 5 lb - packaged in clear plastic bags",
      "content_text": "Class III Ongoing\nFirm: Wonton Specialists\nReason: Undeclared FD&C Red No. 40\nDistribution: NY, NJ, PA\nRecall began: 2026-07-28\nFDA IDs: H-1325-2026 / event 99508\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class III",
        "Ongoing"
      ]
    },
    {
      "id": "H-1329-2026",
      "url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22",
      "external_url": "https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22",
      "title": "Food: OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDI...",
      "content_text": "Class I Ongoing\nFirm: Fayus Inc.\nReason: Undeclared milk.\nDistribution: Domestic: CA, GA, IL, NJ, NY, TX Foreign: Canada, Australia\nRecall began: 2026-07-06\nFDA IDs: H-1329-2026 / event 99368\nSource: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22",
      "date_published": "2026-09-09T00:00:00.000Z",
      "tags": [
        "Food",
        "Class I",
        "Ongoing"
      ]
    }
  ]
}