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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.

37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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
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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 9,521–9,540 of 20,769 recalls

FDA Recall Terminated Historical recordClass II

DrKids Children's Natural Cough Syrup English Ivy Leaf, packaged in Pre-measured Single-Use Vials 0.17 fl. oz. (5 mL) Each 3.4 fl. oz. (100 mL), Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321 UPC 370302489026

by Unipharma, Llc.

Reason
CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, packaged in a 8 fl oz (237 mL) bottle, Rx only, Manufactured By Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053. NDC 60432-212-08

by Morton Grove Pharmaceuticals, Inc.

Reason
Failed Impurities/Degradation Specifications - failed specs for Prednisolone Impurity 14
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 300mg 30 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2865-31

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 150mg 500 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ 08540 Product of India NDC 0781-2855-05

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sandoz Ranitidine Hydrochloride Capsules 150mg 60 Capsules Rx Only Manufactured by Sandoz Inc. Princeton, NJ Product of India NDC 0781-2855-60

by Sandoz, Inc

Reason
CGMP Deviations: Detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA).
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Major Infants' Gas Relief Drops, Simethicone Oral Suspension USP, 1 FL OZ (30 mL) bottle, Distributed by: Major Pharmaceuticals 17177 N Laurel Park Drive, Suite 233 Livonia, MI 48152 USA. NDC 0904-5894-30

by GCP Laboratories Inc

Reason
Microbial Contamination of Non-Sterile Product.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Premo and Fresh Grab brands Tuna Salad, refrigerated 5 oz.…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Premo and Fresh Grab brands Egg Salad, refrigerated 5 oz. w…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Premo and Fresh Grab brands Chicken Salad, refrigerated 5 o…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Fresh Grab brand Turkey No Cheese, refrigerated 5 oz. wheat…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Fresh Grab brand Ham & Cheese, refrigerated 5 oz. wheat bre…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass I

Lipari Foods Operating Company, LLC.

Product
Premo brand Bologna & Cheese Wedge, refrigerated 5 oz. wedg…
Reason
FDA environmental sampling returned a positive test result for Listeria monocytogenes.
Published
October 16, 2019
Distribution
FL IL IN KY MD MI OH PA TN WI…

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FDA Recall United States Terminated Historical recordClass II

Vinh Sanh Trading Corp

Product
Tep Say Crispy Tiny Shrimp Snack, Net Wt. 7 oz. in plastic j…
Reason
Undeclared sulfites.
Published
October 16, 2019
Distribution
U.S. distribution to the following: MI,…

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FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Gridestone Cafe Swiss Style Cocoa Mix, Net Wt. 32 OZ (2 lb)…
Reason
Products were made with a cocoa powder that contained soy lecithin but soy was not declared on the label.
Published
October 16, 2019
Distribution
Distributed to customers in CA, CO, CT,…

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FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Chef's Companion Instant Chocolate Mousse Mix Net Wt. 1 lb 1…
Reason
Products were made with a cocoa powder that contained soy lecithin but soy was not declared on the label.
Published
October 16, 2019
Distribution
Distributed to customers in CA, CO, CT,…

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FDA Recall United States Terminated Historical recordClass II

Diamond Crystal Brands Inc

Product
Madrona Market Delicatessen Hot Cocoa Mix, Net Wt. 2 lb (907…
Reason
Products were made with a cocoa powder that contained soy lecithin but soy was not declared on the label.
Published
October 16, 2019
Distribution
Distributed to customers in CA, CO, CT,…

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FDA Recall United States Terminated Historical recordClass II

Abbott Laboratories

Product
Abbott Calcilo XD, Low-calcium Vitamin D-Free Infant formula…
Reason
Off color and odor. Compromised can seam due to product (powder) in the seam, this poor seal potentially allowed air into the container.
Published
October 16, 2019
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

STARK INC.

Product
Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffe…
Reason
Product contains undeclared milk.
Published
October 16, 2019
Distribution
Products were distributed in: NY, OH, CA…

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FDA Recall Terminated Historical recordClass II

Phenylephrine Hydrochloride Ophthalmic Solution, USP, 2.5%, 15 mL bottle, Rx only, Mfd. by: Akorn, Inc., Lake Forest, IL 60045; NDC 17478-201-15.

by Akorn, Inc.

Reason
Lack of Assurance of Sterility: Out of specification results for container closure test which cannot guarantee the sterility of the product.
Published
October 9, 2019
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Losartan Potassium/ Hydrochlorothiazide Tablets, USP 100mg/25mg, 90 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-118-90

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.
Published
October 9, 2019
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.