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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 12,221–12,240 of 20,777 recalls

FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Au Jus Seasoning Reduced…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Salt & Vinegar Seasoning…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Premix Roasted Chicken 12…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Roasted Wing Marinade Seaso…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Fire Roasted Steak Type S…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Toasted Italian Herbs 66112…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Pan Roast Brown Gravy Mix 6…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass II

GRIFFITH FOODS

Product
Product Name Lot Number or ID Whiskey & Cola Type Flavore…
Reason
Griffith Foods, Inc. has initiated a voluntary recall of multiple products following a supplier's recall of Autolyzed Yeast Powder due to the presence of Salmonella.
Published
April 4, 2018
Distribution
Domestic: IL, TX, VA, WI, OK, MS Fore…

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FDA Recall United States Terminated Historical recordClass I

Taylor Farms California Foodservice, Inc.

Product
Taylor Farms 3/8" Diced Yellow Onion 4/5# bags - 20 lb, corr…
Reason
Firm was notified by direct customer of a confirmed positive result for Salmonella ssp. after routine testing of the diced onion product.
Published
April 4, 2018
Distribution
OK, OH, MI, MN, IA, CA, KS, WI, PA, OR,…

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FDA Recall Terminated Historical recordClass III

Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.

by Akorn, Inc.

Reason
Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published
March 28, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

Ikea North America Srvcs Inc

Product
Pink flexible, plastic package: Godis Paskkyckling Marshm…
Reason
Possible Pest Contamination at production facility.
Published
March 28, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Valacyclovir Tablets USP 1 gram, 30-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India NDC # 31722-705-30

by Hetero Labs Limited Unit V

Reason
Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Valganciclovir Tablets, USP, 450 mg, 60-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India. NDC # 31722-832-60

by Hetero Labs Limited Unit V

Reason
Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets, USP 5/1.5 mg Rx Only 30 Tablets Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-118-03 UPC 343386118038

by Novel Laboratories, Inc.

Reason
Failed Impurities/Degradation Specifications
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Stability Specifications:Out-of-specification results observed for viscosity during stability testing.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL 60045 USA. NDC: 0409-2634-01

by Pfizer Inc.

Reason
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618. NDC: 0703-0110-01

by Pfizer Inc.

Reason
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sermorelin Acetate, powder, a) 1 GM-bottle (NDC58597-8092-1) b) 5 GM-bottle (NDC 58597-8092-2) c) 10 GM-bottle (NDC 58597-8092-4) API American Pharmaceutical Ingredients

by American Pharmaceutical Ingredients LLC

Reason
Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin USP, powder, 1g-bottle, API American Pharmaceutical Ingredients, NDC 58597-7042-3

by American Pharmaceutical Ingredients LLC

Reason
Stability Data Does Not Support Expiry: Stability data from manufacturer does not support expiration dates listed.
Published
March 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.

by Alva-Amco Pharmacal Companies., Inc.

Reason
Subpotent Drug: The product has failed to maintain its label claim of coal tar throughout its labeled 24-month expiry period.
Published
March 21, 2018
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.