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Recall totals

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

37,269

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-farmstead-dairy-announces-recall-raw-mild-cheddar-cheese-due-potential-e-coli-o157h7Published October 15, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 17, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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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FDA Recall OngoingHistorical recordClass II

Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy

by Boothwyn Pharmacy LLC

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

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FDA Recall United States TerminatedTerminated: March 31, 2026Historical recordClass II

Jessie Lord Bakery, LLC

Product: Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate aft…
Reason: Undeclared Yellow#5 in Lemon Meringue Pie
Published: September 10, 2025
Distribution: Product is distributed across the follow…

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FDA Recall United States TerminatedTerminated: January 21, 2026Historical recordClass II

TAMPA MAID FOODS, LLC

Product: Clean-tail Coconut Farm Raise Breaded Butterfly Shrimp Clean…
Reason: Product may be contaminated with Cesium-137 (Cs-137)
Published: September 10, 2025
Distribution: Product was distributed to OH, MI, WI, P…

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FDA Recall United States TerminatedTerminated: January 21, 2026Historical recordClass II

TAMPA MAID FOODS, LLC

Product: ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC (SYSCO) Cle…
Reason: Product may be contaminated with Cesium-137 (Cs-137)
Published: September 10, 2025
Distribution: Product was distributed to OH, MI, WI, P…

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FDA Recall United States TerminatedTerminated: January 21, 2026Historical recordClass II

TAMPA MAID FOODS, LLC

Product: Panko Style Breaded Butterfly Shrimp (16/20 CT per pound) in…
Reason: Product may be contaminated with Cesium-137 (Cs-137)
Published: September 10, 2025
Distribution: Product was distributed to OH, MI, WI, P…

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Data last updated: October 17, 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.