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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,561–5,580 of 18,718 recalls

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

View recall →

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 II

LILY'S SWEETS LLC

Product
Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
Reason
Lily s Sweets, LLC has initiated a recall of Lily s Peppermint Flavor Baking Chips , 7 oz. pouch, 6 pouches per case, corrugated case because the presence of soy lecithin.
Published
February 16, 2022
Distribution
Product Distributed to the following Sta…

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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 United States Terminated Historical recordClass II

Amys Kitchen Inc

Product
Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g)…
Reason
Firm investigation detected trace amounts of milk through finished product testing.
Published
February 16, 2022
Distribution
Distributed in United States: AL, AR, AZ…

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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

View recall →

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

View recall →

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

View recall →

FDA Recall Terminated Historical recordClass II

SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets, 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

View recall →

FDA Recall Terminated Historical recordClass II

AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) tablets, 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

View recall →

FDA Recall Terminated Historical recordClass II

CETAFEN Extra Non-Aspirin Pain Relieve (Acetaminophen 500 mg) caplets, 2-count packets, Manufactured for: HARTHealth Seattle, WA 98124

by Ultra Seal Corporation

Reason
cGMP deviations
Published
February 9, 2022
Distribution
Nationwide

View recall →

Data last updated:

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.