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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.

37,204
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).
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 13,341–13,360 of 21,084 recalls

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

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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FDA Recall United States Terminated Historical recordClass I

Commonwealth Dairy, Llc

Product
Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt, 5.…
Reason
Recalling Friendly Farms Key Lime Crunch Tilts because it may contain undeclared almond pieces.
Published
August 30, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bush Brothers & Co

Product
BUSHS BEST¿ Original SEASONED WITH BACON & BROWN SUGAR BAKED…
Reason
During an FDA inspection the firm was informed that cans may have defective side seams which may cause the cans to leak or allow for growth of C. botulinum..
Published
August 30, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Bush Brothers & Co

Product
BUSHS BEST¿ Country Style THICK, RICH SAUCE WITH BACON & EXT…
Reason
During an FDA inspection the firm was informed that cans may have defective side seams which may cause the cans to leak or allow for growth of C. botulinum..
Published
August 30, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Bush Brothers & Co

Product
BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BR…
Reason
During an FDA inspection the firm was informed that cans may have defective side seams which may cause the cans to leak or allow for growth of C. botulinum.
Published
August 30, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Penobscot McCrum LLC

Product
Medium Coated Jo-Jo Wedges / 00040 (5lb bags)
Reason
Product may contain undeclared milk.
Published
August 30, 2017
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By: LifeLine Nutrients Corp, 1801 S. Canal St, Chicago, IL 60616, UPC 021754905076

by Global Marketing Enterprises, Inc.

Reason
Marketed without an Approved NDA/ANDA: The product consists of pure, powdered caffeine and is an unapproved drug due to stimulant claims. The product is also misbranded as it fails to bear adequate directions for its intended use.
Published
August 23, 2017
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass III

Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12

by AVKARE Inc.

Reason
Failed impurities/degradation specifications: Out of specification for a related compound C.
Published
August 23, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin Pharmaceuticals, Inc., Baltimore, MD, 21202

by Lupin Limited (Unit 1)

Reason
Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.
Published
August 23, 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.