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Recall totals

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

37,271

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 recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 19, 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 United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Poblano packaged as 5lb half sliced with 2 bags per case, 5l…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Jalapeno peppers packaged as 5lb diced with 2 bags per case,…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Freshire Farms - Green Peppers packaged in plastic bags cont…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Freshire Farms - Green Beans packaged in plastic bags at 1lb…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Freshire Farms - Jalapenos packaged in plastic bags at 8oz,…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall TerminatedTerminated: June 12, 2025Historical recordClass II

Gabapentin Tablets, USP, 600 mg, 500-count bottles, Rx only, Manufactured by: Granules India Limited Hyderabad-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA NDC 70010-227-05

by Granules Pharmaceuticals Inc.

Reason: Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: May 7, 2025Historical recordClass I

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

by A-S Medication Solutions LLC

Reason: Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 28, 2025Historical recordClass II

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064

by EMPOWER CLINIC SERVICES LLC

Reason: Lack of Assurance of Sterility
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass III

Methotrexate Tablets, USP, 2.5mg, 100-count Bottle, RX Only, Distributed By: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC# 69238-1423-1

by Amneal Pharmaceuticals, LLC

Reason: Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall TerminatedTerminated: April 28, 2025Historical recordClass III

PEG-3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Sodium Ascorbate, and Ascorbic Acid for Oral Solution 100g/7.5 g /2.691 g/1.015 g/ 5.9 g / 4.7 g, 3 pouches/carton, Rx only, Distributed by: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC# 0093-3560-26.

by Novel Laboratories, Inc. d.b.a Lupin Somerset

Reason: Defective container: potential for non-sealed pouches which can lead to product leakage.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass I

Umary Acido Hialuronico, Suplemento Alimenticio, 850 mg caplets, packaged in 30-count bottles.

by MAIN PRODUCTS INC

Reason: Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Published: August 14, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass III