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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,060

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

State: MD ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 9, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass III

Dynamic Sports Nutrition

Product: Anabolic Research WINN-50 (vanazolol). Dietary Supplement.…
Reason: Dietary supplement involved degradation of an ingredient. Product is sub-potent for Vitamin B12 not meeting label claims.
Published: September 17, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Wegmans Food Markets, Inc.

Product: Wegmans Caramel Apple Pecan Topped Brie Cheese -Small - 13 O…
Reason: Products may be contaminated with Listeria monocytogenes
Published: September 17, 2025
Distribution: NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…

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FDA Recall United States Terminated Historical recordClass I

Wegmans Food Markets, Inc.

Product: Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes…
Reason: Products may be contaminated with Listeria monocytogenes
Published: September 17, 2025
Distribution: NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…

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FDA Recall United States Terminated Historical recordClass I

Wegmans Food Markets, Inc.

Product: Wegmans Assorted Cheese Flight - Varies (sold by the lb) - B…
Reason: Products may be contaminated with Listeria monocytogenes
Published: September 17, 2025
Distribution: NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…

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FDA Recall United States Terminated Historical recordClass I

Wegmans Food Markets, Inc.

Product: Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round…
Reason: Products may be contaminated with Listeria monocytogenes
Published: September 17, 2025
Distribution: NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…

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FDA Recall Ongoing Historical recordClass I

0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7800-09

by B BRAUN MEDICAL INC

Reason: Presence of Particulate Matter.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Lactated Ringers's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07

by B BRAUN MEDICAL INC

Reason: Presence of Particulate Matter
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100-count bottles Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1062-1.

by Amneal Pharmaceuticals, LLC

Reason: Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1060-1.

by Amneal Pharmaceuticals, LLC

Reason: Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1058-1.

by Amneal Pharmaceuticals, LLC

Reason: Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottles, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1056-1.

by Amneal Pharmaceuticals, LLC

Reason: Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg, Double Strength, Rx Only, Packaged as a) 100-count bottle, NDC 65162-272-10; b) 500-count bottle, NDC 65162-272-50; Manufactured by: Amneal Pharmaceuticals, Pvt. Ltd, Oral Solid Dosage Unit, Ahmedabad, 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807.

by Amneal Pharmaceuticals, LLC

Reason: Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore Commercial LLC, 181 Washington St, Conshohocken, PA, 19428, Product of Denmark NDC 80446-0401-01 Lot #: 3D009AA09, 3D009AA10, 3D009AA25, Exp Date: 31 MAR 2026 NDC 80446-0401-99 (Non-Commercial FG) Lot #: 3D009AA02, Exp Date 31 MAR 2026

by IMMUNOCORE, LLC

Reason: Subpotent Drug
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08

by DermaRite Industries, LLC

Reason: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34

by DermaRite Industries, LLC

Reason: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08

by DermaRite Industries, LLC

Reason: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) bag-n-box (NDC 61924-092-27) and b) 1000ml (34 fl. oz.) bag-n-box (NDC 61924-092-34) , DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy

by Boothwyn Pharmacy LLC

Reason: Subpotent Drug
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy

by Boothwyn Pharmacy LLC

Reason: Subpotent Drug
Published: September 10, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496

by Boothwyn Pharmacy LLC

Reason: Subpotent Drug
Published: September 10, 2025
Distribution: Nationwide

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Data last updated: September 9, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.