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Recall totals

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

37,204
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
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 13,721–13,740 of 21,402 recalls

FDA Recall Terminated Historical recordClass II

Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85

by The Harvard Drug Group

Reason
Microbial contamination of Non-sterile Products; presence of yeast and potential B. cepacia contamination
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Phentermine Capsules, 15 mg, a) 7-count bottle (NDC 55289-791-07), b) 14-count bottle ( NDC 55289-791-14), c) 21-count bottle (NDC 55289-791-21), d) 30-count bottle (NDC 55289-791-30), e) 60-count bottle (NDC 55289-791-60), Packaged by PD-Rx Pharmaceuticals, Incorporated, Oklahoma City, OK. 73127 Mfg: KVK-Tech, Inc. Newtown, PA 18940

by PD-Rx Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications:Out of specification results for individual unknown impurities at 30th month Room Temperature Retained Sample stabilities test .
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

by C. O. Truxton

Reason
Labeling: Label Mixup; potentially mislabeled
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharmaceuticals Huntsville, AL 35811, Distributed by: Truxton, Inc. Bellmawr, NJ 08031, NDC: 0463-6352-10

by C. O. Truxton

Reason
Labeling: Label Mixup; potentially mislabeled
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031

by C. O. Truxton

Reason
Labeling: Label Mixup; potentially mislabeled
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6151-10

by C. O. Truxton

Reason
Labeling: Label Mixup; potentially mislabeled
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10

by C. O. Truxton

Reason
Labeling: Label Mixup; potentially mislabeled
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

by C. O. Truxton

Reason
Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

The Best Bar Ever Inc.

Product
The Best Bar Ever, Peanut Butter Crunch, 1.41 oz., 40 gm.
Reason
The Best Bar Ever initiated a voluntary recall of the Peanut Butter Crunch flavor (40g size) because the individual wrapper mistakenly has a gluten-free logo on the label. The wrapper for Peanut Butter Crunch flavor (40g size), had a gluten-free logo on the individual wrapper label. The ingredient listing and allergen statements are correct. The only issue is the gluten-free icon was not supposed to be on that flavor.
Published
August 30, 2017
Distribution
Domestic Only: FL and GA

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FDA Recall United States Terminated Historical recordClass II

Lakeside Foods, Inc

Product
IQF Green Beans, Keep Frozen. 11 varieties, packaged under…
Reason
IQF French Style Green Beans and IQF Cut Green Beans may be contaminated with Listeria monocytogenes.
Published
August 30, 2017
Distribution
Distributors in 17 states: WI, TN, KY, O…

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Broaster Recipe Crinkle Cut Seasoned Wedges / 96698 (5 lb ba…
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb…
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Extra Large Seasoned/Battered Jo-Jo Wedges / 00148 (5 lb bag…
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Medium Seasoned/Battered Jo-Jo Wedges / 00129 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Seasoned/Battered Baby Jo-Jo Wedges / 00049 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Extra Large Coated Jo-Jo Wedges / 00048 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Battered Jo-Jo Wedges / 00047 (5 lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass III

Grandma's Herbs

Product
"Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Die…
Reason
Grandmas Herbs Cholesterol has undeclared soy lecithin.
Published
August 30, 2017
Distribution
Nationwide

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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.