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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 October 2026.

37,206
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 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)

  • 1,714 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 15,161–15,180 of 21,652 recalls

FDA Recall United States Terminated Historical recordClass III

Moondance Heavenly Desserts, LLC

Product
Moondance desserts gluten free Mexican Wedding Cookie 8 oz (…
Reason
undeclared pecans
Published
May 24, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Moondance Heavenly Desserts, LLC

Product
Moondance desserts gluten free Chocolate Chip Cookie Bar 12…
Reason
undeclared milk
Published
May 24, 2017
Distribution
Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

McCain Foods USA

Product
Wegman's O'Brien Hash Browns, frozen packages, net wt. 28 o…
Reason
Wegman's O'Brien Hash Browns product, lot B161021, is recalled because it may contain golf ball materials, specifically hard plastic or rubber pieces.
Published
May 24, 2017
Distribution
Distributed in Maryland, Massachusetts,…

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FDA Recall Terminated Historical recordClass II

Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-4359-93), Individual Blister Pack (NDC 0093-4359-19), Rx Only, Manufactured By: Teva Pharmaceutical Industries Ltd., Jerusalem, 9777600, Israel

by Teva Pharmaceuticals USA

Reason
Microbial Contamination of Non-Sterile Products
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

PrednisoLONE Oral Solution USP, 15 mg/5mL, alcohol content: 5%(v/v) 240 mL bottle, Rx Only, Manufactured in Canada By: CONTRACT PHARMACEUTICALS LIMITED CANADA, Ontario, Canada, L5N 6L6, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-6118-87

by Teva Pharmaceuticals USA

Reason
Failed Stability Specifications
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (NDC 62756-556-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India.

by Sun Pharmaceutical Industries, Inc.

Reason
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 10 mg, packaged in a) 30-count bottles (NDC 62756-554-83), b) 100-count bottles (NDC 62756-554-88), and c) 1000-count bottles (NDC 62756-554-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India, NDC 62756-551-18.

by Sun Pharmaceutical Industries, Inc.

Reason
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-count bottles (NDC 62756-553-88), and c) 1000-count bottles (NDC 62756-553-18), Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, 350 Gujarat, India.

by Sun Pharmaceutical Industries, Inc.

Reason
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Olanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-551-18.

by Sun Pharmaceutical Industries, Inc.

Reason
Failed Impurities/Degradation Specifications: out of specification results for the related substances test parameter (impurities).
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Buprenorphine HCI Injection, 0.3 mg/mL, 1 mL Single Dose Vial (NDC 42023-179-01), packaged in 1 mL x 5 Single Dose Vials per carton (NDC 42023-179-05), Rx Only, Distributed by: Par Pharmaceuticals Companies, Inc., Spring Valley, NY 10977.

by Par Sterile Products LLC

Reason
Crystallization: due to the presence of white, crystalline particulates, adhered to the side and bottom of the glass vials, which are comprised of principally dextrose and the buprenorphine active component.
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powder, Rx only, Manufactured by: Akorn, Inc., NDC 17478-701-02

by Akorn, Inc.

Reason
Product is being recalled due to low pH value.
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
32 count Miss Vickies Multipack Box 44 oz. packaged in flexi…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
30 count Lays Kettle Cooked Multipack Tray 41.25 oz. package…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
30 count Miss Vickies Multipack Tray 41.25 oz. packaged in f…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexib…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Frito-Lay, Inc

Product
Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape…
Reason
Potential presence of Salmonella
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Vertical Pharmaceuticals, Inc.

Product
Vertical Pharmaceuticals OB Complete with DHA Prenatal Multi…
Reason
One (1) lot (21511158) of the OB Complete DHA is being recalled because the label claim for "Omega-3 Fatty Acids" does not match the actual formulation.
Published
May 17, 2017
Distribution
AL, AR, AZ, CA, CO, FL, GA, IL, LA, MA,…

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FDA Recall United States Terminated Historical recordClass II

Treehouse Foods

Product
Macaroni & Cheese microwaveable cups sold under the followin…
Reason
Products containing cheddar cheese seasoning which may be contaminated with Salmonella.
Published
May 17, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Pinnacle Foods, LLC

Product
Great Value Bread and Butter Chips 24 Fl Oz. Distributed b…
Reason
Glass fragments were found in Great Value Bread and Butter Chips.
Published
May 17, 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.