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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.

37,063
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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 2,641–2,660 of 18,346 recalls

FDA Recall Terminated Historical recordClass I

Odor-Eaters Spray Powder, Tolnaftate 1% Antifungal, packaged in a) 4 oz. aerosol cans (UPC 0 41388 0041 2, NDC 10157-4645-1) and b) 5.3 oz. aerosol cans (UPC 0 41388 00411 2, NDC 10157-4645-2) Blistex P.O. Box 5392, Oak Brook, IL 60522-5392.

by Blistex Inc

Reason
Chemical contamination: Presence of benzene
Published
December 27, 2023
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Phenytoin Oral Suspension, USP, 100 mg/4 mL, packaged in packaged in 4 mL unit dose cups (NDC 0904-7079-24), 50 per case (NDC 0904-7079-57), Rx only, Major Pharmaceuticals Livonia, MI 48152

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason
Failed Content Uniformity Specifications
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass I

TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.

by Insight Pharmaceuticals Corporation

Reason
Chemical Contamination; presence of benzene.
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Raw Seafoods Inc.

Product
Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs c…
Reason
Contains undeclared sesame seeds and milk
Published
December 27, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Kenover Marketing Corp.

Product
Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53…
Reason
Undeclared milk due to mispackaging
Published
December 27, 2023
Distribution
Distributed to distributors and retailer…

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FDA Recall Terminated Historical recordClass II

Liothyronine Sodium Tablets, USP 5 mcg, 100-count bottle, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. NDC 62756-589-88

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Impurities/Degradation Specifications
Published
December 20, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass III

Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried Barbera, S.L., Barbera del Valles, Spain, Distributed by: Novartis Pharmaceuticals Corp., East Hanover, N.J. 07936, NDC 0078-1077-66

by Siegfried Barbera, SL

Reason
Failed Dissolution Specifications
Published
December 20, 2023
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

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FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

View recall →

FDA Recall United States Terminated Historical recordClass I

Houdini Inc.

Product
Acorn Raspberry Creme Filled Cookie found in gift basket: #…
Reason
Undeclared allergens; tree nuts
Published
December 20, 2023
Distribution
U.S. distribution to the following: AK,…

View recall →

FDA Recall Completed Historical recordClass II

ROPivacaine HCl 0.2% PF in Sodium Chloride 1,000 mg/500 mL (2 mg per mL) Injection, 500 mL bags, Rx only, STAQ Pharma Inc. 14135 E 42nd Ave, Unit 50, Denver, Colorado 80239, NDC 73177-0109-26,

by STAQ Pharma, Inc.

Reason
STAQ Pharma Inc. received consumer complaints related to leaking bags and other potential bag concerns. Upon investigation, they determine the source of the issue was with the bag manufacturer who released bags Lot # 134142-001A which had failed internal QC tests for leaks.
Published
December 13, 2023
Distribution
Nationwide

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FDA Recall Completed Historical recordClass II

Ondansetron Injection, USP, 4 mg/2 mL (2 mg/mL), 2 mL per vial, Rx only, Manufactured for: Baxter Healthcare Corporation, Deerfield, IL 60015 USA. Manufactured by: Baxter Pharmaceuticals India Private Ltd, Ahmedabad 382213, India. NDC 36000-012-25

by Baxter Healthcare Corporation

Reason
Failed pH Specifications
Published
December 13, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

SANDIMMUNE Oral Solution (cyclosporine oral solution, USP) 100 mg/mL, 50 mL bottle, Rx Only, Manufactured by: DELPHARM Huningue S.A.S., Huningue, France, Distributed by: Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. NDC 0078-0110-22

by Novartis Pharmaceuticals Corporation

Reason
Crystallization: bottles of Sandimmune Oral Solution were determined to contain crystals
Published
December 13, 2023
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

KinderMed INFANTS' PAIN & FEVER Acetaminophen, 160 mg per 5 mL bottles, Oral Suspension, Organic Cherry Flavor, 2 FL OZ (59 mL), Distributed By: KinderFarms, Redondo Beach, CA 90277, NDC 82673-096-02, UPC 850001805698.

by KINDER FARMS LLC

Reason
Failed Impurities/Degradation Specifications
Published
December 13, 2023
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.