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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 18, 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 II

Lorazepam Tablets, USP, 2mg, Unit Dose, 100 tablets per carton (10 x 10 blister packs), Rx only, The drug product contained in this package is from NDC # 69315-906 Leading Pharma, LLC., Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 26268 USA, NDC: 0904-6009-61.

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Published: February 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Lorazepam Tablets, USP, 1mg, Unit Dose, 100 tablets per carton (10 x 10 blister packs), Rx only, The drug product contained in this package is from NDC # 69315-905 Leading Pharma, LLC., Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 26268 USA, NDC: 0904-6008-61.

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Published: February 26, 2025
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Lorazepam Tablets, USP, 0.5mg, Unit Dose, 100 tablets per carton (10 x 10 blister packs), Rx only, The drug product contained in this package is from NDC # 69315-904 Leading Pharma, LLC., Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 26268 USA, NDC: 0904-6007-61

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities.
Published: February 26, 2025
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

fentaNYL Citrate In Sodium Chloride 1600mcg/100mL (16 mcg per mL) CII, Single use 100mL IV Bag, Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67726 Bar Code 71266-5060-01

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility
Published: February 26, 2025
Distribution: Distributed in PA

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FDA Recall United States TerminatedTerminated: August 7, 2025Historical recordClass II

United Natural Trading Inc. dba Woodstock Farms

Product: Wegmans, Organic Almonds Dry Roasted Salted, 12oz clear bag,…
Reason: Product mislabeled. The back label states Organic Cashews. The front product label states Wegmans Organic unsalted dry roasted almonds. The front label is correct label for this product.
Published: February 26, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States TerminatedTerminated: August 19, 2026Historical recordClass II

GLOBAL COMMODITIES INC

Product: AAHU BARAH brand SOFT PLUM; NET WT. 0.5 LB; Import By: AAHU…
Reason: Product contains undeclared sulfites (4.66 mg/serving).
Published: February 26, 2025
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: May 28, 2025Historical recordClass II

Feel Good Foods Inc

Product: Feel Good Foods; Three Cheese Mac & Cheese Bites; NET WT 8oz…
Reason: Foreign object (metal pieces).
Published: February 26, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 24, 2026Historical recordClass II

Shata Traders Inc.

Product: THREE RIVERS brand TUTTI-FRUTTI; INGREDIENTS Papaya Cubes, S…
Reason: Product contains undeclared FD&C Yellow 5 and FD&C Yellow 6.
Published: February 26, 2025
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Irbesartan Tablets USP, 300 mg, 50 Tablets (5 x 10) Unit Dose per carton, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 50268-442-15

by AvKARE

Reason: Out of Specification for Dissolution
Published: February 19, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 22, 2025Historical recordClass I

Wismettac Asian Foods, Inc.

Product: Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK,…
Reason: Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Published: February 19, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 22, 2025Historical recordClass I

Wismettac Asian Foods, Inc.

Product: Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK,…
Reason: Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Published: February 19, 2025
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: July 22, 2025Historical recordClass I