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Recall totals

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

37,210

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 3, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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 United States Terminated Historical recordClass II

Pharmatech LLC

Product: CytoDetox, Hydrolyzed Clinoptilolite Fragments, 1 oz./30 mL,…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Renew HC, Hydrolyzed Clinoptilolite, 1 oz./30 mL, OTC Non-St…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Pedia Poly-Vite Drops, 50 mL, OTC Non-Sterile. Dietary supp…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Pedia Tri-Vite Drops with Iron, 50 mL, OTC Non-Sterile. Die…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Ferrous Drops, 50 mL, OTC Non-Sterile. Dietary supplement.
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Poly-Vita Drops with Iron, 50 mL, OTC Non-Sterile. Dietary…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Poly-Vita Drops, 50 mL, OTC Non-Sterile. Dietary supplement…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Polyvitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplem…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dieta…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary suppleme…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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FDA Recall United States Terminated Historical recordClass II

Pharmatech LLC

Product: Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL,…
Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Published: November 2, 2016
Distribution: FL, MI, MS, and OH.

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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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FDA Recall United States Terminated Historical recordClass III

National Foods Packaging Inc

Product: National Foods Packaging Low Sodium Chicken Base in 50 lb wh…
Reason: Product contains a spice which was tested and found to contain elevated levels of lead.
Published: October 26, 2016
Distribution: Nationwide

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Data last updated: October 3, 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.