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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 6,481–6,500 of 22,605 recalls

FDA Recall Terminated Historical recordClass II

Losartan Potassium Tablets, USP 25 mg, 90 Tablets bottles, Rx Only Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-163-90 UPC 3 72789 16390 1

by PD-Rx Pharmaceuticals, Inc.

Reason
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Independent Beverage Company LLC

Product
PurAqua Belle Vie SPARKLING WATER wellness RELAX 100mg ASHWA…
Reason
Firm indicated that the product contains undeclared caffeine.
Published
July 6, 2022
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Wilton Industries Inc

Product
Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 71…
Reason
Milk contamination
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Wilton Industries Inc

Product
Wilton Rainbow Sprinkles Mix net wt 5.92 oz. item number 71…
Reason
Milk contamination
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. W…
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Fudgeamentals LLC

Product
PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz.
Reason
made with peanut butter contaminated with Salmonella
Published
July 6, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Stellex/CF Houston, LLC

Product
Wegman's Apple, Pretzels & Cheese with Peanut Butter Net Wt…
Reason
Potential to be contaminated with Salmonella
Published
July 6, 2022
Distribution
VA, TN, NC, SC, FL, GA, PA, NJ, DE, MA,…

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FDA Recall United States Terminated Historical recordClass I

Stellex/CF Houston, LLC

Product
Giant Apples, Pretzels & Celery with peanut butter Net Wt. 4…
Reason
Potential to be contaminated with Salmonella
Published
July 6, 2022
Distribution
VA, TN, NC, SC, FL, GA, PA, NJ, DE, MA,…

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FDA Recall United States Terminated Historical recordClass I

Stellex/CF Houston, LLC

Product
Snack Sensations Apple, Pretzel & Celery Bites with Peanut B…
Reason
Potential to be contaminated with Salmonella
Published
July 6, 2022
Distribution
VA, TN, NC, SC, FL, GA, PA, NJ, DE, MA,…

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FDA Recall United States Terminated Historical recordClass I

Stellex/CF Houston, LLC

Product
Snack Fresh Apple & Cheese Bites with Crackers Net Wt. 4 oz.…
Reason
Potential to be contaminated with Salmonella
Published
July 6, 2022
Distribution
VA, TN, NC, SC, FL, GA, PA, NJ, DE, MA,…

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FDA Recall United States Terminated Historical recordClass I

Stellex/CF Houston, LLC

Product
Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed i…
Reason
Potential to be contaminated with Salmonella
Published
July 6, 2022
Distribution
VA, TN, NC, SC, FL, GA, PA, NJ, DE, MA,…

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FDA Recall Terminated Historical recordClass II

Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.

by Teva Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications; Low Out of Specification (OOS) results for dissolution.
Published
June 29, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Failed Tablet/Capsule Specification; oversized tablet found in a bottle
Published
June 29, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Lack of Assurance of Sterility: Manufacturing deviation which was reported due to a microbial excursion
Published
June 29, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, 1 mL Single-dose vial per carton, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification for impurities.
Published
June 29, 2022
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.