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

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Source: FDA and USDA public dataLast updated September 14, 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 I

MAC DADDY PURPLE Capsules, packaged in 10-count blisters per carton, ASIN B08Z63Z4QK, UPC 742137 605764.

by ABC Sales 1 Inc

Reason: Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil and/or sildenafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making these unapproved drugs.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.

by ABC Sales 1 Inc

Reason: Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil and/or sildenafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making these unapproved drugs.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Moxifloxacin Ophthalmic Solution, USP 0.5% w/v, 3 mL bottle, Sterile, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, Made in India, NDC 65862-840-03

by Aurobindo Pharma USA Inc.

Reason: Failed Impurities/Degradation Specifications
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Diazepam Oral Solution (Concentrate), 25 mg per 5 mL (5 mg/mL), 30 mL BOTTLE and DROPPER, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 0527-1768-36.

by Lannett Company, Inc.

Reason: Failed Impurities/Degradation Specifications: Out of specification results for related substances.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

365 SKINNY High Intensity Capsules, 600 mg, 30-count bottle, BODY BALANCE INTERNACIONAL

by Je Dois Lavoir LLC

Reason: Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared sibutramine, a previously approved drug that was withdrawn from the US market due to safety concerns.
Published: February 23, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

HARD DAWN, Rise and Shine capsules, 500 mg, packaged in 10-count blisters per carton, Made in Malaysia, UPC 680044 364926, ASIN: B077XCCL59

by Esupplementsales, LLC

Reason: Marketed Without an Approved NDA/ANDA: Firm was informed by Amazon that analytical testing showed the presence of tadalafil. Tadalafil is a FDA approved drug, making this product an unapproved drug.
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

MegMan Performance Booster, 800 mg capsules, packaged in 10-count blisters packaged in a carton, UPC 8 48998 00091 2, ASIN B08Z74KS88

by Junp Hydration LLC

Reason: Marketed Without An Approved NDA/ANDA: product was found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Polymyxin B for Injection USP, 500,000 Units per Vial, 10 mL vials, packaged in 10 vials per carton, Sterile, Rx Only, Distributed by: AuroMedics Pharma LLC, E. Windsor, NJ 08520, NDC 55150-234-10

by AuroMedics Pharma LLC

Reason: Presence of Particulate Matter; product complaint of hair discovered in a vial within the lot
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Siren Snacks

Product: Siren Birthday Cake Protein Bites, Item # 1104, brand Siren…
Reason: Undeclared cashews and almond butter allergens
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CONAGRA BRANDS

Product: Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-4132…
Reason: Undeclared eggs
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

CONAGRA BRANDS

Product: Wishbone Thousand Island Dressing 15oz. bottle UPC 0-41321-0…
Reason: Undeclared eggs
Published: February 16, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx Only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Manufactured For: Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0093-5455-42

by Teva Pharmaceuticals USA

Reason: Mislabeling
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Mimvey (estradiol and norethindrone acetate tablets USP), 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Manufactured For: Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0093-5455-28

by Teva Pharmaceuticals USA

Reason: Mislabeling
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Tretinoin Capsules, 10 mg, 100 count bottle, Rx Only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0555-0808-02

by Teva Pharmaceuticals USA

Reason: Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution.
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sinus Relief Headache/Nasal (acetaminophen 325mg, phenylephrine HCl 5mg), 2 tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sinus Relief (acetaminophen 325mg, Guaifenesin 200mg, phenylephrine HCl 5mg), 2-tablet packets, Manufactured for Select Corporation, Carrollton, TX 75007

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 mg) Caplets, packaged in 36-count blisters Physician's Seal LLC, Boca Raton, FL 33487

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

REMfresh Advanced Ion-Powered Melatonin (Melatonin 2 mg) Caplets, packaged in a) 12-count blisters b) 36-count blisters Physician's Seal LLC, Boca Raton, FL 33487

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ELECTROLYTE Supplement Tablets (calcium 5.2 mg, Potassium 20.8 mg, Magnesium 6 mg ) 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MIRALAC (calcium carbonate 420mg) tablets, Mint Flavor, 2-count packets, Dist. by Honeywell Safety Products USA, Smithfield, RI 02917

by Ultra Seal Corporation

Reason: cGMP deviations
Published: February 9, 2022
Distribution: Nationwide

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Data last updated: September 14, 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.