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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 October 2026.

37,212
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

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)

  • 1,714 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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,366
Class I9,841
Class III2,892
Not Yet Classified2

Showing 16,261–16,280 of 21,638 recalls

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 Terminated Historical recordClass I

Cetylev (acetylcysteine) effervescent tablets for oral solution, 500 mg, Rx Only, 20 tablets per carton (ten 2 count blister packs), Distributed by Arbor Pharmaceuticals, LLC Atlanta, GA 30328, NDC 24338-700-10.

by Arbor Pharmaceuticals Inc.

Reason
Defective Container: Incomplete seal on blister packaging, leading to tablet swelling and enlarging due to effervescence process beginning as oxygen and moisture enter the blister packaging.
Published
October 26, 2016
Distribution
CA, FL, GA, LA, MO, MS, NC, OH, PA, SC,…

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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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FDA Recall United States Terminated Historical recordClass III

National Foods Packaging Inc

Product
National Foods Packaging Chicken Base in 25 lb white poly-li…
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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FDA Recall United States Terminated Historical recordClass III

National Foods Packaging Inc

Product
Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined b…
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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FDA Recall United States Terminated Historical recordClass II

King Henry's, Inc.

Product
Gummy Frogs, 6oz, UPC 6105465200, 61054645500
Reason
King Henry is recalling King Henry's Gummy Frogs because they may contain undeclared colors (FD&C Yellow #6, Yellow #5, Red #40).
Published
October 26, 2016
Distribution
US: CA, OH, TX, CO

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FDA Recall United States Terminated Historical recordClass II

King Henry's, Inc.

Product
Gummy Frogs, 2.5oz, UPC 61054635210
Reason
King Henry is recalling King Henry's Gummy Frogs because they may contain undeclared colors (FD&C Yellow #6, Red #40).
Published
October 26, 2016
Distribution
US: CA, OH, TX, CO

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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.