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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

State: MT ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 28, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Persantine (dipyridamole USP) tablets, 75 mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877, NDC 0597-0019-01

by Boehringer Ingelheim Pharmaceuticals, Inc.

Reason: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in a 75 mg Persantine 100-count bottle and 50 mg Persantine tablet was found in a 100 count bottle of 75 mg Dipyridamole.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Ferrara Candy Comp

Product: BRACH'S Chocolate Creations, Milk Chocolate Almond Supremes,…
Reason: Undeclared peanuts and wheat in product.
Published: November 2, 2016
Distribution: NE, WI, IL, IN, WA, MO, IA, FL, MN, OH,…

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Teal Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Purple Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Pink Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Silver Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color found to contain mold, yeast or bacteria
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Blue Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color found to contain mold, yeast, or bacteria
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Bob's Red Mill Natural Foods, Inc.

Product: Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM…
Reason: The firm is voluntarily recalling one lot of Guar Gum due to due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Brown Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Green Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Yellow Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Red Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Pearl Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Gold Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color has the potential to be contaminated with mold, yeast or bacteria.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Brands.

Product: Wilton Black Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
Reason: Airbrush color found to contain mold, yeast or bacteria
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Mccormick

Product: Club Size McCormick Original Taco Seasoning Mix 24 oz. , C…
Reason: Product was recalled due to undeclared milk.
Published: November 2, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Trokendi XR (topiramate) extended-release capsule, 50mg, 30-count blister pack, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850, NDC 17772-102-15

by Supernus Pharmaceuticals, Inc.

Reason: Superpotent Drug: Failure of assay specifications in the capsule.
Published: October 26, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PARICALCITOL Capsules, 4 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7658-56.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
Published: October 26, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PARICALCITOL Capsules, 2 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7657-56.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
Published: October 26, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

PARICALCITOL Capsules, 1 mcg, 30-count bottles, Rx only, Manufactured By: Pharmaceutics International, Inc., Hunt Vallet, MD 21031; Manufactured For: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0093-7656-56.

by Teva Pharmaceuticals USA

Reason: Failed Impurities/Degradation Specifications: out of specification test results for impurities during stability testing.
Published: October 26, 2016
Distribution: Nationwide

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Data last updated: September 28, 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.