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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
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
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 12,521–12,540 of 18,563 recalls

FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Strawberry Rhubarb Cobbler, One Pint…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Chocolate Peanut Butter Pretzel, One…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Creamy Dark Chocolate Mint, One Pint…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Vanilla Bean, One Pint, UPC 41483-04…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Salted Caramel Brownie, One Pint, UP…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps Sweet Me Creamery Expresso Mocha, One Pint, UPC 41483-…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Raspberry Cheesecake, One Pint, UPC…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Chocolate Peanut Butter Fudge, One P…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Very Vanilla, One Pint, UPC 41483-04…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Salty Caramel Cookie Crunch, One Pin…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Cold Brewed Coffee, One Pint, UPC 41…
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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FDA Recall United States Terminated Historical recordClass II

Kemps, LLC

Product
Kemps YO2 Frozen Yogurt Mudslide, One Pint, UPC 41483-04121
Reason
Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.
Published
May 24, 2017
Distribution
AL, CA, FL, IA, IL, LA, MA, MD, MI, MN,…

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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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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.