BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Not Yet Needed//Recall Radar//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Recall Radar latest recalls
X-WR-CALDESC:Recent FDA food, drug, supplement, and medical device recalls from public openFDA enforcement data.
BEGIN:VEVENT
UID:Drugs-99837-20260916@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Drugs recall: fentaNYL Citrate\, 1\,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL\, 0.9% NaCl Bag\,...
DESCRIPTION:Not Yet Classified Ongoing Firm: OurPharma LLC Reason: 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). Distribution: Nationwide within the U.S Recall began: 2026-09-03 FDA IDs: / event 99837 Source: https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=event_id%3A%2299837%22
END:VEVENT
BEGIN:VEVENT
UID:D-0836-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Drugs recall: Fluphenazine Hydrochloride Tablets\, USP\, 1mg\, 100-count bottles\, Rx Only\, Marketed by: Aja...
DESCRIPTION:Class III Ongoing Firm: Ajanta Pharma USA Inc Reason: 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. Distribution: Nationwide within the U.S Recall began: 2026-08-25 FDA IDs: D-0836-2026 / event 99733 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0836-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0835-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Drugs recall: Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution\, 10 mL per dropper bottl...
DESCRIPTION:Class III Ongoing Firm: ImprimisRx NJ LLC Reason: Subpotent Drug Distribution: USA Nationwide Recall began: 2026-08-24 FDA IDs: D-0835-2026 / event 99756 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0835-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1341-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Food recall: Alfalfa\, Net Weight 50 lbs. bag\, Product of USA\, International Specialty Supply 1011 Volun...
DESCRIPTION:Class I Ongoing Firm: International Sprout Holdings\, Inc Reason: Potential E. coli and Salmonella contamination Distribution: 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 Recall began: 2026-08-23 FDA IDs: H-1341-2026 / event 99822 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1341-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0850-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Drugs recall: Dextrose Injection\, USP\, 70 %\, 2000 mL bags\, Rx Only\, Baxter Healthcare Corporation Deerfi...
DESCRIPTION:Class I Ongoing Firm: Baxter Healthcare Corporation Reason: Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. Distribution: U.S. Nationwide. Recall began: 2026-08-17 FDA IDs: D-0850-2026 / event 99679 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0850-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1334-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Food recall: Fannie May & XO Marshmallow Pixie S'mores Collection\, 4.47oz
DESCRIPTION:Class II Ongoing Firm: Ferrero USA Reason: Undeclared milk and pecans Distribution: IA\, IL\, IN\, OH Recall began: 2026-08-14 FDA IDs: H-1334-2026 / event 99682 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1334-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1330-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Food recall: Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower\, net wt. 3oz (85g). UPC 6...
DESCRIPTION:Class I Ongoing Firm: EXOTIQUE FOODS CANADA Reason: Undeclared Wheat. Distribution: Product was sold in the U.S. Recall began: 2026-08-07 FDA IDs: H-1330-2026 / event 99636 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1330-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1335-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Food recall: Prolon Everyday Apulian Almond & Cocoa Spread\, NET WT: 8.47 OZ. Product packaged in glass...
DESCRIPTION:Class II Ongoing Firm: L-Nutra Inc Reason: Undeclared allergen (tree nuts): hazelnut\, cashew\, and pistachio. Distribution: Product is sold exclusively from the recalling firm's online website nationwide. Recall began: 2026-08-07 FDA IDs: H-1335-2026 / event 99675 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1335-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3111-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Getinge PVC Thoracic Catheter\, Soft PVC Straight\, 10 per Case\; Size(Model Number): 1. 16FR...
DESCRIPTION:Class II Ongoing Firm: Atrium Medical Corporation Reason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. Distribution: US Nationwide distribution. Recall began: 2026-08-07 FDA IDs: Z-3111-2026 / event 99680 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3111-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3113-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Getinge PVC Thoracic Catheter\, Firm PVC Straight\, 10 per Case\; Size(Model Number): 1. 28FR...
DESCRIPTION:Class II Ongoing Firm: Atrium Medical Corporation Reason: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. Distribution: US Nationwide distribution. Recall began: 2026-08-07 FDA IDs: Z-3113-2026 / event 99680 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3113-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3110-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that d...
DESCRIPTION:Class II Ongoing Firm: Lutronic Corporation Reason: Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment\, potentially resulting in patient burn. Distribution: Worldwide distribution - US Nationwide and the countries of Canada and European Union. Recall began: 2026-08-06 FDA IDs: Z-3110-2026 / event 99601 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3110-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3133-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201
DESCRIPTION:Class II Ongoing Firm: Nipro Renal Soultions USA\, Corporation Reason: Hemodialysis concentrates contain high endotoxin levels Distribution: 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. Recall began: 2026-08-05 FDA IDs: Z-3133-2026 / event 99573 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3133-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3134-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X\, 36.83X\, 45X))
DESCRIPTION:Class II Ongoing Firm: Nipro Renal Soultions USA\, Corporation Reason: Hemodialysis concentrates contain high endotoxin levels Distribution: 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. Recall began: 2026-08-05 FDA IDs: Z-3134-2026 / event 99573 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3134-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3136-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D\,LC+201\, LC+225(45X)
DESCRIPTION:Class II Ongoing Firm: Nipro Renal Soultions USA\, Corporation Reason: Hemodialysis concentrates contain high endotoxin levels Distribution: 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. Recall began: 2026-08-05 FDA IDs: Z-3136-2026 / event 99573 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3136-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1331-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Food recall: Crown Farms Dried Suri Cut\, 200 gm\, in plastic pack\, 25 packages per box\, keep frozen
DESCRIPTION:Class I Ongoing Firm: EURO FOODS GROUP USA NJ INC Reason: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying. Distribution: The adulterated product was distributed to the following states: VA\, NY\, NJ\, MI Recall began: 2026-08-01 FDA IDs: H-1331-2026 / event 99684 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1331-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3138-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: AMS Convenience Kit: DSAEK Pack - RX\, Part Number AMS12394B
DESCRIPTION:Class II Ongoing Firm: Windstone Medical Packaging\, Inc. Reason: 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. Distribution: US Nationwide distribution in the states of CA\, GA\, WA. Recall began: 2026-07-29 FDA IDs: Z-3138-2026 / event 99658 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3138-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3120-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: HeartSine SAM 350P 350P US Device\, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P...
DESCRIPTION:Class II Ongoing Firm: HeartSine Technologies Ltd Reason: Due to a damaged (over stretched) membrane tail that causes an intermittent fault. Distribution: 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\,... Recall began: 2026-07-27 FDA IDs: Z-3120-2026 / event 99568 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3120-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3114-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914...
DESCRIPTION:Class II Ongoing Firm: C.R. Bard Inc Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. Distribution: 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... Recall began: 2026-06-25 FDA IDs: Z-3114-2026 / event 98840 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3114-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3115-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Fo...
DESCRIPTION:Class II Ongoing Firm: C.R. Bard Inc Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. Distribution: 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... Recall began: 2026-06-25 FDA IDs: Z-3115-2026 / event 98840 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3115-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3118-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter...
DESCRIPTION:Class II Ongoing Firm: C.R. Bard Inc Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. Distribution: 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... Recall began: 2026-06-25 FDA IDs: Z-3118-2026 / event 98840 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3118-2026%22
END:VEVENT
BEGIN:VEVENT
UID:Z-3119-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260916
DTEND;VALUE=DATE:20260917
SUMMARY:Devices recall: Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex...
DESCRIPTION:Class II Ongoing Firm: C.R. Bard Inc Reason: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. Distribution: 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... Recall began: 2026-06-25 FDA IDs: Z-3119-2026 / event 98840 Source: https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3119-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0833-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Trokendi XR\, (topiramate) extended-release capsules\, 50 mg\, 30 Capsules\, Rx only\, Manufact...
DESCRIPTION:Class III Ongoing Firm: Supernus Pharmaceuticals\, Inc. Reason: Failed dissolution specifications. Distribution: US Nationwide. Recall began: 2026-08-31 FDA IDs: D-0833-2026 / event 99767 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0833-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0834-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: traZODone Hydrochloride Tablets\, USP\, 50 mg\, Rx only\, 100 Tablets\, Manufactured in Croatia...
DESCRIPTION:Class II Ongoing Firm: Teva Pharmaceuticals USA\, Inc Reason: Presence of Foreign Tablets/Capsules Distribution: U.S. Nationwide Recall began: 2026-08-24 FDA IDs: D-0834-2026 / event 99734 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0834-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0840-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Buprenorphine Sublingual Tablets (C-III)\, 2 mg\, 30 Tablets (3x10)\, Rx only\, Distributed by...
DESCRIPTION:Class III Ongoing Firm: American Health Packaging Reason: Labeling: Label Mix-up Distribution: US Nationwide. Recall began: 2026-08-19 FDA IDs: D-0840-2026 / event 99674 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0840-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1304-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Prince ITALIAN BREAD\; Sesame\; NET WEIGHT 8 OZ. (227g)\; INGREDIENTS: ENRICHED BLEACHED FLOU...
DESCRIPTION:Class III Ongoing Firm: Prince Bakery Inc Reason: Sesame is not declared in the ingredient statement but is declared in the statement of identity. Distribution: New York. Recall began: 2026-08-13 FDA IDs: H-1304-2026 / event 99646 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1304-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1305-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Prince ITALIAN BREAD\; Sesame\; ITALIAN & FRENCH BREAD\, LARGE\; NET WEIGHT 12 OZ. (340g)\; ING...
DESCRIPTION:Class III Ongoing Firm: Prince Bakery Inc Reason: Sesame is not declared in the ingredient statement but is declared in the statement of identity. Distribution: New York. Recall began: 2026-08-13 FDA IDs: H-1305-2026 / event 99646 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1305-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0811-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Vasopressin\, in 0.9% Sodium Chloride Injection\, 20 units per 100 mL (0.2 units/mL)\, 100mL...
DESCRIPTION:Class II Ongoing Firm: Baxter Healthcare Corporation Reason: CGMP Deviations Distribution: US Nationwide\; Puerto Rico\; and Chile. Recall began: 2026-08-06 FDA IDs: D-0811-2026 / event 99500 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0811-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0813-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection\, 40 mg in 200 mL...
DESCRIPTION:Class II Ongoing Firm: Baxter Healthcare Corporation Reason: CGMP Deviations Distribution: US Nationwide\; Puerto Rico\; and Chile. Recall began: 2026-08-06 FDA IDs: D-0813-2026 / event 99500 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0813-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0815-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Clindamycin Injection USP in 5% Dextrose\, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Sing...
DESCRIPTION:Class II Ongoing Firm: Baxter Healthcare Corporation Reason: CGMP Deviations Distribution: US Nationwide\; Puerto Rico\; and Chile. Recall began: 2026-08-06 FDA IDs: D-0815-2026 / event 99500 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0815-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0821-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Daptomycin\, in 0.9% Sodium Chloride Injection\, 1\,000 mg per 100 mL (10 mg/mL)\, 1\,000 mg to...
DESCRIPTION:Class II Ongoing Firm: Baxter Healthcare Corporation Reason: CGMP Deviations Distribution: US Nationwide\; Puerto Rico\; and Chile. Recall began: 2026-08-06 FDA IDs: D-0821-2026 / event 99500 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0821-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1308-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Weis (Fresh From the Orchard ) Pasteurized Apple Cider\, Contains 100 % Juice\, the product...
DESCRIPTION:Class II Ongoing Firm: WEIS MARKETS\, INC. Reason: Product has high patulin levels Distribution: The recalled product was distributed to the State of PA. Recall began: 2026-08-06 FDA IDs: H-1308-2026 / event 99638 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1308-2026%22
END:VEVENT
BEGIN:VEVENT
UID:D-0851-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Drugs recall: Glutathione 200 mg/mL\, 30 mL sterile multidose vial\, Each vial contains: Glutathione\, Asco...
DESCRIPTION:Class I Ongoing Firm: OPTIMAL BALANCE PHARMACY Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. Distribution: USA Nationwide. Recall began: 2026-08-05 FDA IDs: D-0851-2026 / event 99662 Source: https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0851-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1327-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Ho...
DESCRIPTION:Class II Ongoing Firm: Ukrop's Homestyle Foods LLC Reason: Foreign object: metal fragments Distribution: Product was shipped to the following states: KY\, NC\, VA & WVA. Recall began: 2026-07-30 FDA IDs: H-1327-2026 / event 99548 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1327-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1320-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Wonton Specialist Inc. Pan Fried Noodle\, 16 oz and 5lb packaged in clear plastic bags
DESCRIPTION:Class III Ongoing Firm: Wonton Specialists Reason: Undeclared FD&C Red No. 40 Distribution: NY\, NJ\, PA Recall began: 2026-07-28 FDA IDs: H-1320-2026 / event 99508 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1320-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1325-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: Wonton Specialist Inc. Cooked Noodle\, 16 oz and 5 lb - packaged in clear plastic bags
DESCRIPTION:Class III Ongoing Firm: Wonton Specialists Reason: Undeclared FD&C Red No. 40 Distribution: NY\, NJ\, PA Recall began: 2026-07-28 FDA IDs: H-1325-2026 / event 99508 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1325-2026%22
END:VEVENT
BEGIN:VEVENT
UID:H-1329-2026@notyetneeded.com
DTSTAMP:20260924T003029Z
DTSTART;VALUE=DATE:20260909
DTEND;VALUE=DATE:20260910
SUMMARY:Food recall: OLA-OLA Pounded Yam (Iyan) IYANINSTANT\, NET WT. 2 lbs.\, 4 lbs.\, 5 lbs.\, 10 lbs\, packed in...
DESCRIPTION:Class I Ongoing Firm: Fayus Inc. Reason: Undeclared milk. Distribution: Domestic: CA\, GA\, IL\, NJ\, NY\, TX Foreign: Canada\, Australia Recall began: 2026-07-06 FDA IDs: H-1329-2026 / event 99368 Source: https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22 For awareness only. Confirm details with FDA\, the recalling firm\, or a clinician before making medical decisions.
URL:https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1329-2026%22
END:VEVENT
END:VCALENDAR