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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 13, 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

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 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

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FDA Recall Terminated Historical recordClass II

Accuretic (quinapril HCl/hydrochlorothiazide) tablets, 20 mg/12.5 mg*, 90 Tablets, Rx Only, Distributed by: Parke-Davis, Division of Pfizer Inc., NY. NY 10017, Made in Germany, NDC 0071-5212-23 .

by Pfizer Inc.

Reason: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Published: April 13, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

quinapril HCl/hydrochlorothiazide tablets, 20 mg/25 mg*, 90 Tablets, Rx Only, Distributed by: Greenstone, LLC, Peapack, NJ, 07977, Made in Germany, NDC 59762-0223-1

by Pfizer Inc.

Reason: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide impurity above the acceptable daily intake limit.
Published: April 13, 2022
Distribution: Nationwide

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Data last updated: September 13, 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.