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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: RI ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 12, 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 Terminated Historical recordClass II

Ampicillin and Sulbactam for Injection, USP 1.5 grams per vial, Rx only, Mfd for Meitheal Pharmaceuticals Chicago, IL 60631, NDC 71288-005-20

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 1g per vial, Rx only, Manufactured for: Xellia Pharmaceuticals USA, LLC, Buffalo Grove, IL 60089, NDC 70594-086-02

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP 2g per vial, Rx only, Mfg. for: Piramal Critical Care, Bethlehem, PA 18017 USA, NDC 66794-223-41

by Astral SteriTech Private Ltd.

Reason: Lack of Assurance of Sterility
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Admelog, insulin lispro injection, 100 units/mL (U-100), 3mL multi-dose vial, Rx Only, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807 A Sanofi Company. NDC 0024-5926-05

by Sanofi-Aventis U.S. LLC

Reason: Lack of Assurance of Sterility: Malformed crimped collar seal
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

General Mills, Inc

Product: Gold Medal Bleached All Purpose Flour, Enriched, Presifted,…
Reason: Flour has the potential to be contaminated with Salmonella.
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

General Mills, Inc

Product: Gold Medal Unbleached All Purpose Flour, Enriched, Presifted…
Reason: Flour has the potential to be contaminated with Salmonella.
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Big Bold Health Holdings Inc

Product: Microbiome Rejuvenate dietary supplement, 60 capsules per bo…
Reason: Glass fragments.
Published: May 24, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Gabapentin Tablets, USP 600 mg, packaged in Cartons of 100 tablets (10 tablets per blister pack x 10), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. East Windsor, NJ 08520 Distributed by: Major Pharmaceuticals 17177 N Laurel Park Dr., Suite 233 Livonia, MI 48152 USA, NDC 0904-6823-61

by The Harvard Drug Group

Reason: Product mixup: one foreign tablet found in product.
Published: May 17, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Calcitonin Salmon (synthetic origin) Nasal Spray, 2200 USP Calcitonin Salmon Units/mL, 200 USP Calcitonin Salmon Units/spray, 3.7 mL bottle, Rx only, Manufactured by: Apotex Corp., Toronto, Ontario, Canada, M9L 1T9, NDC 60505-0823-6

by Apotex Corp.

Reason: Presence of Foreign Substance: Glass splinter particle entrapped inside the pump ball seat rendered the pump inoperable.
Published: May 17, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.

by Camber Pharmaceuticals Inc.

Reason: Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.
Published: May 17, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Euro-Pharma

Product: Multiple Vitamin B Capsules, 60 Capsules, Biologically Activ…
Reason: undeclared allergen (milk)
Published: May 17, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Pro Power Knight Plus capsule, 2550mg, 1-count blister card, Distributed by Beyond Health and youth Inc, Seattle, WA 98110, UPC 4 94922 90522 0.

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles.

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.

by Family Dollar Stores, Llc.

Reason: CGMP deviation: product outside labeled storage temperature requirements.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Simvastatin USP 40 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottle (NDC 43063-0726-30) b) 90 count-bottle (NDC 43063-0726-90)

by PD-Rx Pharmaceuticals, Inc.

Reason: CGMP deviations.
Published: May 10, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Simvastatin USP 20 mg, Rx only, Intas Pharm. Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottles (NDC 43063-008-30), b) 90 count-bottles (NDC: 43063-0008-90)

by PD-Rx Pharmaceuticals, Inc.

Reason: CGMP deviations.
Published: May 10, 2023
Distribution: Nationwide

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Data last updated: September 12, 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.