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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 13, 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

Dollar General Corporation

Product: DG Health brand Sugar Free Daily Fiber in 10 oz. plastic con…
Reason: Product is missing warning declaration that it contains phenylalanine.
Published: March 29, 2023
Distribution: Products were distributed to the followi…

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FDA Recall Terminated Historical recordClass II

Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC 678112000708; NDC 67172-504-01.

by Teva Pharmaceuticals USA Inc

Reason: Failed Impurities Specification: Out-of-specification (OOS) stability test result was obtained for unspecified impurity.
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Buprenorphine Transdermal System, CIII 20 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7079-05

by AVEVA Drug Delivery Systems, Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Buprenorphine Transdermal System, CIII 10 mcg/hour, 4 Transdermal Systems One package of 4 disposal units, Rx Only, Manufactured by: Aveva Drug Delivery Systems Inc. Miramar, FL. 33025, Manufactured for: Apotex Corp Weston, FL. 33326, NDC 60505-7077-05

by AVEVA Drug Delivery Systems, Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification for related substance 10-hydroxy buprenorphine N-Oxide results generated at the 18-month stability timepoint.
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Evamist (estradiol transdermal spray), 1.53 mg of estradiol per spray, 0.27 fl oz (8.1 mL) per metered-dose pump, Rx Only, Manufactured by DPT Laboratories, Ltd San Antonio, TX 78215, Manufactured for: Perrigo, Allegan, Minnapolis, MN 55427, NDC: 0574-2067-27

by Padagis US LLC

Reason: Failed Content Uniformity Specifications: The Spray Content Uniformity (SCU) requirement for Standard Deviation did not meet the requirement at the 18-month stability time point.
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-901-01

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clobazam Tablets, 10 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-900-01

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 2 mg, CIV, packaged in: a)100-count bottle (NDC 51991-0707-01) and b) 500-count bottle (NDC 51991-0707-05), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Potential risk of Cross Contamination
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

KEURIG DR PEPPER

Product: Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-c…
Reason: Product contains black tea, resulting in caffeine being undeclared.
Published: March 22, 2023
Distribution: AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL,…

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Pingo Peanut Butter Cookie Hot Chocolate packaged in single…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.…
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Navada Imports

Product: Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.)…
Reason: Undeclared peanut allergen
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

TWO RIVERS COFFEE LLC

Product: Cold Stone Creamery Hot Cocoa Peanut Butter Cup Perfection p…
Reason: Coffee pods may contain undeclared peanut residue
Published: March 22, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Purely Soothing MSM Nasal Spray, 15%, packaged in 30ml, 1.014 fl. oz bottles, Manufactured by: Pharmedica USA, Phoenix, AZ, UPC 7 31034 91380 5

by Pharmedica USA, LLC

Reason: CGMP Deviations
Published: March 15, 2023
Distribution: Nationwide

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Data last updated: September 13, 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.