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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.

37,205
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/gias-foods-inc-recalls-bettergoods-authentic-italian-lemon-alfredo-fettuccine-because-possible-0Published October 1, 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 14,921–14,940 of 21,084 recalls

FDA Recall United States Terminated Historical recordClass I

Bickel's Snack Foods Inc

Product
Seyfert-Sour Cream & Onion Flavored Potato Chips sold in 2…
Reason
Bickel's Snack Foods, Inc. of York, PA is voluntarily recalling all snack products that were made with milk ingredients supplied by one of its' secondary seasoning component suppliers.
Published
February 15, 2017
Distribution
Shipped to VT, NJ, NY, FL, MI, WI, and V…

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FDA Recall United States Terminated Historical recordClass I

Bickel's Snack Foods Inc

Product
Bon Ton-Sour Cream & Onion Flavored Potato Chips sold in 2.…
Reason
Bickel's Snack Foods, Inc. of York, PA is voluntarily recalling all snack products that were made with milk ingredients supplied by one of its' secondary seasoning component suppliers.
Published
February 15, 2017
Distribution
Shipped to VT, NJ, NY, FL, MI, WI, and V…

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FDA Recall United States Terminated Historical recordClass II

The Dannon Company, Inc.

Product
DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles…
Reason
The label incorrectly states "WALNUT" in the ingredient list and the allergen statement, while the product actually contains PECAN as an ingredient.
Published
February 15, 2017
Distribution
Arizona, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass I

Subco Foods of Wisconsin, Inc.

Product
Best Choice Pistachio Instant Pudding & Pie Filling, UPC 0 7…
Reason
Subco Foods of Wisconsin was notified by their supplier, that the high heat nonfat dry milk powder, an ingredient that they supplied, was being recalled due to possible Salmonella contamination.
Published
February 15, 2017
Distribution
TN, MO,OH, KS, WI, MI, PA, IN, IL, NC, O…

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FDA Recall United States Terminated Historical recordClass I

Subco Foods of Wisconsin, Inc.

Product
Best Choice Lemon Instant Pudding & Pie Filling UPC 0 70038…
Reason
Subco Foods of Wisconsin was notified by their supplier that the high heat nonfat dry milk powder, an ingredient that they supplied, was being recalled due to possible Salmonella contamination.
Published
February 15, 2017
Distribution
TN, MO,OH, KS, WI, MI, PA, IN, IL, NC, O…

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FDA Recall United States Terminated Historical recordClass I

Subco Foods of Wisconsin, Inc.

Product
Best Choice French Vanilla Instant Pudding & Pie Filling, UP…
Reason
Subco Foods of Wisconsin was notified by their supplier that the high heat nonfat dry milk powder, an ingredient from that they supplied, was being recalled due to possible Salmonella contamination.
Published
February 15, 2017
Distribution
TN, MO,OH, KS, WI, MI, PA, IN, IL, NC, O…

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FDA Recall United States Terminated Historical recordClass I

Subco Foods of Wisconsin, Inc.

Product
Bakers Corner Vanilla Instant Pudding & Pie Filling, UPC 0 4…
Reason
Subco Foods of Wisconsin was notified by their supplier that the high heat nonfat dry milk powder, an ingredient that they supplied, was being recalled due to possible Salmonella contamination.
Published
February 15, 2017
Distribution
TN, MO,OH, KS, WI, MI, PA, IN, IL, NC, O…

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FDA Recall United States Terminated Historical recordClass I

Dutch Valley Food Distributors Inc.

Product
Cappuccino Snack Mix Lot code: 20161027; Best By: 05/25/17…
Reason
As a result of an ingredient supplier recall, Dutch Valley is issuing a recall on Cappuccino Snack Mix due to the potential for it to be contaminated with Salmonella.
Published
February 15, 2017
Distribution
DE FL GA IA ID IL IN KS MA MD…

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FDA Recall Terminated Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-711-16.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II (Sugar Free), 1 liter (1000 mL), 4 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-695-79.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Methadone Hydrochloride Oral Concentrate, USP 10 mg/mL C-II, a.) 1 fl. oz. (30 mL), 12 bottles per case (NDC No. 66689-695-30), b). 1 liter (1000 mL), 4 bottles per case, (NDC No. 66689-695-79), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL, a). 5 mL, 50 unit dose cups of 5 mL per case (NDC No. 66689-401-50), b). 500 mL, 12 bottles per case (NDC No. 66689-403-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lactulose Solution, USP 10 g/15 mL, 50 unit dose cups of 15 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-039-50.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lactulose Solution, USP 20 g/30 mL, 50 unit dose cups of 30 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-038-50.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL per case (NDC No. 66689-037-50), b). 100 unit dose cups of 5 mL per case (NDC 66689-037-99), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Phenytoin Oral Suspension, USP 100 mg/ 4 mL, 50 unit dose cups of 4 mL per case., Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-036-50.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/325 mg per 15 mL C-II, a) 4 fl.oz .(120 mL), 12 bottles per case (NDC 66689-023-04), b) 16 fl.oz. (473 mL), 12 bottles per case (NDC 66689-023-16), c) 50 unit dose cups of 15 mL per case, (NDC No. 66689-023-50), Rx only, Manufactured by VistaPharm, Largo, FL 33771

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 bottles per case (NDC 66689-008-02), b) 16 fl. oz. (237 mL), 12 bottles per case (NDC 66689-008-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771

by VistaPharm, Inc.

Reason
CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.
Published
February 8, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

MIDAZOLAM INJECTION, USP, *25 mg/5 mL, (5 mg/ mL), 5 mL vials, 10 Vials per carton, Rx only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- NDC 63323-412-05

by Fresenius Kabi USA, LLC

Reason
Failed Impurities/Degradation Specifications
Published
February 8, 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.