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Recall totals

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

37,324

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 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: FL ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 21, 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	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall OngoingHistorical recordClass II

Safe tussin PM, NIGHT TIME Cough Relief, (Dextromethorphan HBr, USP 7.5mg, Doxylamine Succinate 3.125mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.

by Denison Pharmaceuticals, LLC

Reason: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Published: June 7, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Pin-Away PYRENTAL PAMOATE (Pyrantel base 50 mg / mL) Pinworm Treatment, 2 FL OZ (60 mL) bottle, Distributed by: Cara Incorporated, 333 Strawberry Field Road, Warwick, RI 05886. NDC 70309-080-02

by Denison Pharmaceuticals, LLC

Reason: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Published: June 7, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: October 7, 2024Historical recordClass II

Vital Proteins

Product: Vital Proteins Collagen Peptides, retail 24oz plastic canist…
Reason: potential foreign material contamination (pieces of one blue broken lid may be in one or more canisters)
Published: June 7, 2023
Distribution: Distributed to retail locations in the f…

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

GARDEN HIGHWAY ATLANTA

Product: TURKEY AND HAVARTI Sandwich NET WT. 8.55OZ (242g) CONTAINS M…
Reason: During an internal audit the firm discovered that the label did not declare sesame in their ingredient statement.
Published: June 7, 2023
Distribution: Product was shipped to the following sta…

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FDA Recall United States TerminatedTerminated: August 21, 2024Historical recordClass I

AH USA Group Inc

Product: Black Fungus Golden Koi 2.5 oz packages 100 bags per case UP…
Reason: Product may contain salmonella
Published: June 7, 2023
Distribution: Product distributed in PA, CA, FL, MN, W…

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FDA Recall United States TerminatedTerminated: December 8, 2023Historical recordClass I

Living Nutz Living Organic Foods

Product: Living Nutz Nut & Seed Butter Raw Sprouted & Stoneground; 8…
Reason: Nut butter potentially contaminated by Salmonella.
Published: June 7, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: August 18, 2023Historical recordClass II

Regal Trading, Inc.

Product: Trader Joes Instant Cold Brew Coffee, 3.5 oz.(99g), 24 jars…
Reason: Presence of foreign material (glass particles) in product.
Published: June 7, 2023
Distribution: Multiple states

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FDA Recall OngoingHistorical recordClass II

Tirzepatide 10 mg/0.5 mL Sterile Solution-2 mL Vial, Rx Only, For Sub-Q Use Only, Compounded Drug Product By: Revive Rx, 3831 Golf Dr A, Houston, TX 77018, NDC: 99000-9278-64.

by Revive Rx LLC dba Revive Rx Pharmacy

Reason: Sub-potent Drug
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 29, 2024Historical recordClass III

Fentanyl Buccal Tablets CII, 800mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-638-28

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Incorrect or Missing Package Insert
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 29, 2024Historical recordClass III

Fentanyl Buccal Tablets CII, 600mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-637-28

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Incorrect or Missing Package Insert
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 29, 2024Historical recordClass III

Fentanyl Buccal Tablets CII, 400mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-636-28

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Incorrect or Missing Package Insert
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 29, 2024Historical recordClass III

Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-635-28

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Incorrect or Missing Package Insert
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 29, 2024Historical recordClass III

Fentanyl Buccal Tablets CII, 100mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-634-28

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Incorrect or Missing Package Insert
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall CompletedHistorical recordClass II

Pain Reliever, Acetaminophen USP Caplets, 500 mg, 225-count bottles packaged in a cardboard carton, Distributed by: Walgreen Co., 200 Wilmot Rd, Deerfield, IL 60015; NDC 0363-9947-35.

by Aurobindo Pharma USA Inc.

Reason: Failed Impurities/Degradation Specifications: firm's investigation due to customer complaints for discoloration found that the product was out of specification for an impurity.
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Nafcillin for Injection, USP, 10 gram per Pharmacy Bulk Package, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. NDC: 25021-141-99

by Sagent Pharmaceuticals Inc

Reason: Lack of Assurance of Sterility
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Nafcillin for Injection, USP, 2 gram per vial, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. NDC: 25021-140-10

by Sagent Pharmaceuticals Inc

Reason: Lack of Assurance of Sterility
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall OngoingHistorical recordClass II

Nafcillin for Injection, USP, 1 gram per vial, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195. NDC: 25021-139-10

by Sagent Pharmaceuticals Inc

Reason: Lack of Assurance of Sterility
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: February 27, 2024Historical recordClass II

buPROPrion Hydrochloride Extended-Release Tablets, USP (SR) 150 mg, 60 Tablets, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ, Manufactured by: Sun Pharmaceutical Industries Limited, Gujrat, India, NDC 47335-737-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications; during stability testing
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 6, 2024Historical recordClass II

Glimepiride Tablets, USP, 4 mg, RX, Packaged as a) 100-count bottle, NDC# 68001-179-00; b) 500-count bottle, NDC# 68001-179-03, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories

by Amerisource Health Services LLC

Reason: CGMP Deviations: recalling drug products following an FDA inspection.
Published: May 31, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 6, 2024Historical recordClass II

Glimepiride Tablets, USP, 2 mg, RX, Packaged as a ) 100-count bottle, NDC# 68001-178-00; b) 500-count bottle; NDC# 68001-178-03 Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, INDIA. For BluePoint Laboratories

by Amerisource Health Services LLC

Reason: CGMP Deviations: recalling drug products following an FDA inspection.
Published: May 31, 2023
Distribution: Nationwide

View recall →

Data last updated: October 21, 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.