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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 8,461–8,480 of 17,833 recalls

FDA Recall Terminated Historical recordClass II

Test PROCYP (TESTOSTERONE CYPIONATE 200MG/ML TESTOSTERONE PROPIONATE 20MG/ML), 5 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 MG/ML HYDROXOCOBALAMIN 500 MC/ML DEXPANTHENOL 50 MG/ML PYRIDOXINE HCL 50 MG/ML), 10 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 mL multidose vial compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272

by Customceutical Compounding

Reason
Lack of assurance of sterility for injectables and solutions intended to be sterile.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10

by Advanced Pharma Inc.

Reason
Sub-potency
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-516-15 Manufactured for: AvKARE Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.
Published
May 8, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Dose Rx Only NDC 50268-517-15 Manufactured for: AvKARE Inc. Pulaski, TN 38478

by AVKARE Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 0.96 parts per million.
Published
May 8, 2019
Distribution
Nationwide

View recall →

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…

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

View recall →

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

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.