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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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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 14,461–14,480 of 20,441 recalls

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

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 United States Terminated Historical recordClass III

Yum Retaurants International

Product
Pizza Hut Creamy Alfredo sauce, case size 40 lbs. 8 bags per…
Reason
Foreign object in alfredo sauce. Likely flexible plastic.
Published
February 22, 2017
Distribution
TX. NC, NY, FL, WI, KY, MI, CA, TN, GA,…

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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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FDA Recall Terminated Historical recordClass III

Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ 08810, NDC 55150-202-00

by Aurobindo Pharma USA Inc

Reason
Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.
Published
February 15, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.

by VistaPharm, Inc.

Reason
Defective Container: Leakage of unit dose cups that may occur at the seal.
Published
February 15, 2017
Distribution
Domestic: AL, AZ, CA, CO, CT, FL, GA, HI…

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FDA Recall Terminated Historical recordClass III

Olanzapine tablets, USP, 2.5 mg, packaged in a 30-count bottle, Rx only, Mfd: By: Dr. Reddy's Laboratories Limited, Bachupally, India, NDC 55111-163-30

by Dr. Reddy's Laboratories, Inc.

Reason
Failed impurities/degradation specifications: due to out-of-specification result for the Related Substance Compound C (Impurity 6 - N-Oxide at the 18 month stability station.
Published
February 15, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

Marich Confectionery Company, Inc.

Product
MARICH Premium Chocolates; Chocolate Caramel Heart; Our del…
Reason
Firm received report of customer finding the incorrect product in the Caramel Heart box. The product inside was Triple Chocolate Toffee which contains almonds that are not listed in the Caramel Hearts ingredient list.
Published
February 15, 2017
Distribution
CA, MN and OK.

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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

View recall →

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

View recall →

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.