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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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
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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 14,541–14,560 of 21,142 recalls

FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Trail's End Gourmet Chocolatey Crunch A) NET WT 18 OZ (1.13…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Swirled Pretzels NET WT 5 OZ (141 g) packag…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Bakery Delights Christmas Tree Pretzels NET…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Peppermint Bark A) NET WT 9 OZ (255 g) pack…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies A) Holiday Treats NET WT 15.5 OZ (439 g) pa…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Game Day Party Bowl NET WT 16 OZ (454 g) pa…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Drizzled Peanuts Brittle A) NET WT 8 OZ (22…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Creme De Menthe Bark, A) NET WT 9 OZ (255 g…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Cookies & Cream Bark, NET WT 9 OZ (255 g) p…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
Palmer's Candies Christmas Tree Pretzel, NET WT 7 OZ (198 g)…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall United States Terminated Historical recordClass I

Palmer and Company, dba Palmer Candy Co

Product
A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255…
Reason
Product contains an ingredient that was recalled by a supplier because it may be contaminated with Salmonella
Published
March 1, 2017
Distribution
Product distributed to grocery stores an…

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FDA Recall Terminated Historical recordClass II

Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA 18960.

by Teva Pharmaceuticals USA

Reason
Failed Impurities/Degradation Specifications: out of specification test results for the norethindrone impurity.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17

by ACCORD HEALTHCARE, INC.

Reason
Failed tablet/capsule specification: missing break line on the 5mg tablet.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension, 0.005%/0.064%, packaged in (a) 60 g (NDC 50222-501-06), and (b)120 g (50222-501-66) tubes, Rx Only, Manufactured by: LEO Laboratories Ltd., 285 Cashel Road, Dublin 12 Ireland, Distributed by: LEO Pharma Inc. 1 Sylvan Way, Parsippany, NJ 07054.

by LEO PHARMA INC

Reason
Labeling: Incorrect or missing package insert: the affected product was packaged with an out-of-date package insert (PI) dated February 2014.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-0900-30, UPC 3-0591090030-4

by Actavis Inc

Reason
Failed Dissolution Specifications. Above out of specification for dissolution rate observed at the 10 hour testing point.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130 North, Dayton, NJ 08810 Manufactured by: Aurobindo Pharma Limited Hyderabad-500 072 India, NDC 65862-527-30

by Aurobindo Pharma USA Inc

Reason
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

NOW Foods

Product
NOW¿ Multi-Food 1 Tablets, One Tablet Daily, 90 tablets, A D…
Reason
Product's supplement fact panel incorrectly states that the product contains 75 mg (milligrams) of Molybdenum, when it actually contains 75 mcg (micrograms).
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Bwi Inc

Product
Burts British Hand Cooked Potato Chips Sea Salt & Malted Vi…
Reason
Product is labeled as gluten free; however was labeled as containing an ingredient with gluten.
Published
February 22, 2017
Distribution
U.S. distribution to the following; MA,…

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FDA Recall United States Terminated Historical recordClass II

The Two Little Guys Company

Product
Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Di…
Reason
Joe Chips Sour Cream & Toasted Onion Retro Potato Chips contains a seasoning with a milk powder ingredient that may be contaminated with Salmonella although firm testing has not revealed the presence of the bacteria.
Published
February 22, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Aripiprazole Tablets, 2 mg, 30-count bottle, Rx only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada, M9L 1T9; Manufactured for: Apotex Corp., Weston, Florida 33326, NDC 60505-3075-3.

by Apotex Inc.

Reason
Superpotent Drug: Product may not meet specifications throughout shelf life.
Published
February 15, 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.