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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.

37,066
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

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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 4,721–4,740 of 17,208 recalls

FDA Recall Terminated Historical recordClass II

Rifampin for Injection, USP, 600 mg/vial, One Vial per carton, Rx only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., NDC 67457-445-60

by MYLAN PHARMACEUTICALS INC

Reason
Failed Impurities/Degradation Specifications: High out of specification results obtained for related compound during stability testing.
Published
April 27, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01

by Preferred Pharmaceuticals, Inc.

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability study program.
Published
April 27, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09

by Preferred Pharmaceuticals, Inc.

Reason
Out of specification results observed in dissolution during long term stability testing.
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Cyanocobalamin Injection, USP, 1,000 mcg per mL, For IM or SC Use Only, 1 mL Vial, Rx Only, Manufactured in India, for Auromedics Pharma LLC, NDC 55150-364-01.

by Aurobindo Pharma USA Inc.

Reason
Subpotent Drug: Out of Specification results for Assay
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use, 5mL Single Dose Vial, Rx Only, Teva Pharmaceuticals, USA, Inc., North Wales, PA 19454, NDC 0703-4154-11.

by Teva Pharmaceuticals USA Inc

Reason
Presence of Particulate Matter: Product was found to contain silica and iron oxide
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Industries Inc

Product
Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC:…
Reason
Milk is missing from the product's allergen Contains statement
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Ittella International, LLC

Product
Tattooed Chef Plant-Based Sausage Breakfast Bowl Frozen 18…
Reason
A gluten free claim was inadvertently used on the lid of the container. However, the ingredient statement declares enriched wheat flour as an ingredient and the allergen information statement disclosed the presence of EGGS, WHEAT, MILK, SOY, COCONUT, in bolded text.
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 744-4930, Gordon Choice Southern Style Fish Breader.…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 744-4875, Gordon Choice Yellow Cake Mix. Product is…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 722-0105, Krusteaz Cinnamon Crumb Cake. Product is s…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 721-1000, Krusteaz Belgian Waffle Mix. Product is sh…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 743-0278, IHOP Pancake. Product is shelf stable and…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 731-0120, Krusteaz Pro Buttermilk Pancake Mix. Produ…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 721-0200, Krusteaz Buttermilk Pancake Mix. Product i…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 714-5000, Great Value Buttermilk Pancake & Waffle Mix…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Continental Mills (Corporate Office)

Product
Item # 714-0706, Kroger Buttermilk Pancake & Waffle Mix. Pr…
Reason
foreign materials
Published
April 20, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Cequa (cyclosporine ophthalmic solution) 0.09%, packaged in 6 pouches x 10 single-use vials (0.25 mL each) per box, Manufactured for Sun Pharma Global FZE by: Laboratoire Unither, ZI de la Guerie, F-50211 Coutances Cedex, France, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 47335-506-96

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Subpotent Drug and Presence of Particulate Matter: low out-of-specification results obtained for assay and the presence of particulate matter.
Published
April 13, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-131-02.

by Adamis Pharmaceuticals Corporation

Reason
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Published
April 13, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

SYMJEPI (epinephrine injection, USP) 0.3 mg, (0.3 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA 92130; Distributed by USWM, LLC., Louisville, KY 40241, Made in Belgium, NDC 78670-130-02

by Adamis Pharmaceuticals Corporation

Reason
Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.
Published
April 13, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., BAddi, HImchal Pradesh, INDIA, NDC 33342-107-07.

by Macleods Pharma Usa Inc

Reason
FAILED CONTENT UNIFORMITY SPECIFICATIONS
Published
April 13, 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.