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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.

37,118
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 8,721–8,740 of 18,163 recalls

FDA Recall United States Terminated Historical recordClass II

Frial SAS

Product
Trader Joe's Saucy Scallops with Mushrooms, NET Wt. 16 oz. (…
Reason
Scallop flavor used in the product contains low levels of crustaceans (1 ppm) that is not listed on the product label.
Published
May 8, 2019
Distribution
All US states EXCEPT Alaska, Arkansas, H…

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FDA Recall Terminated Historical recordClass III

Carvedilol Tablets, USP, 3.125 mg, 500-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534; NDC 68382-092-05

by Zydus Pharmaceuticals USA Inc

Reason
Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid, light yellow substance, identified as a fragmented tablet of another drug product, found mixed with tablets in a bottle of Carvedilol tablets 3.125mg.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Fentanyl Citrate Injection, USP, 100 mcg/2 mL (50 mcg/mL), 25 Ampules per carton, (2 mL each), Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-030-25

by Akorn Inc

Reason
Failed impurities/degradation specification: Out of Specification result for total impurity at 4.0% (Limit: NMT 3.0%) at 12 months stability testing.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Mineralife LLC

Product
Trace Minerals Dietary Supplement , 16.2 fl oz (480 mL) bott…
Reason
The dietary supplement product is potentially contaminated with Pseudomonas aeruginosa
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Patagonia Provisions Inc

Product
Patagonia Provisions Savory Seeds Variety Pack; Classic Bar…
Reason
Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Patagonia Provisions Inc

Product
Patagonia Provisions Chipotle Lime Savory Seeds; 1 oz. poly…
Reason
Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Patagonia Provisions Inc

Product
Patagonia Provisions Mellow Curry Savory Seeds; 1 oz. poly-…
Reason
Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Patagonia Provisions Inc

Product
Patagonia Provisions Classic Barbecue Savory Seeds; 1 oz. p…
Reason
Products are labeled gluten free but have been found to contain gluten in excess of 20 ppm in finished products.
Published
May 1, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Remifentanil HCl active pharmaceutical ingredient (API) for manufacturing, processing or repackaging, 416.95 g glass container, Rx ONLY, Johnson Matthey Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, NJ 08066-1742.

by Johnson Matthey Inc.

Reason
Failed Impurities/Degradation Specifications: Unknown impurity above specification limits.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Kopi Jantan Tradisional Natural Herbs Coffee, 13g individual packages, Manufactured By: Fikrysz (M) Sdn. Bhd., Kedah, Malaysia, UPC 9 557205 060083.

by Brian P. Richardson

Reason
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be tainted with undeclared sildenafil and tadalafil, two FDA approved drugs for the treatment of male erectile dysfunction, making this an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amoxicillin for Oral Suspension USP, 125 mg per 5 mL, packaged in (a) 150 mL bottle (NDC 0093-4150-80) (b) 80 mL bottle (NDC 0093-4150-79), Rx Only, Manufactured in Canada By: Teva Canada Limited Toronto, Canada, M1B2K9, Manufactured For: Teva Pharmaceuticals USA, INC. North Wales, PA 19454.

by Teva Pharmaceuticals USA

Reason
Subpotent Product: assay results for Amoxicillin were below the specification limits.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prostaglandin Tri-Mix 30:30:1 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prostaglandin Tri-Mix 20:25:1 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prostaglandin Tri-Mix 2.5:7.5:0.25 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prostaglandin Tri-Mix 5:15:0.5 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenol 10% Injection, 5 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Papaverine 30 mg/mL Injection, 10 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Papaverine 30 mg/Phentolamine 0.5 mg/mL, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HCG 11,00Units/B 12 11,000 mcg Injection, 30 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.

by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy

Reason
Lack of sterility assurance.
Published
April 24, 2019
Distribution
Nationwide

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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.