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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.

37,119
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 10,401–10,420 of 22,138 recalls

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 Completed Historical recordClass I

Sara Lee Frozen Bakery

Product
Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB…
Reason
The firm was notified from a consumer of foreign material in the product. After examination they discovered that the foreign material was "tree nut".
Published
October 16, 2019
Distribution
Product was shipped to the following sta…

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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

SONORA MILLS FOODS INC DBA POPCH

Product
Popchips Variety Pack of Sea Salt, BBQ and Sour Cream and On…
Reason
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Published
October 16, 2019
Distribution
Il, CA, CP. OR, TX, WA, TX, NV, UT, AZ a…

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FDA Recall United States Terminated Historical recordClass II

SONORA MILLS FOODS INC DBA POPCH

Product
Popchips Sea Salt & Vinegar Potato Popped Chips; 5 oz. bag…
Reason
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Published
October 16, 2019
Distribution
Il, CA, CP. OR, TX, WA, TX, NV, UT, AZ a…

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FDA Recall United States Terminated Historical recordClass II

SONORA MILLS FOODS INC DBA POPCH

Product
Popchips Sour Cream & Onion Potato Popped Chips; 5 oz. bag…
Reason
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Published
October 16, 2019
Distribution
Il, CA, CP. OR, TX, WA, TX, NV, UT, AZ a…

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FDA Recall United States Terminated Historical recordClass II

SONORA MILLS FOODS INC DBA POPCH

Product
Popchips Sea Salt Potato Popped Chips; 5 oz. bag, 0.8 oz. ba…
Reason
Some batches of PopChips may contain gluten levels that exceed the firms specification.
Published
October 16, 2019
Distribution
Il, CA, CP. OR, TX, WA, TX, NV, UT, AZ a…

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FDA Recall United States Terminated Historical recordClass II

MOWI USA, LLC

Product
MOWI brand. Whole, head-on gutted farmed, fresh Atlantic Sal…
Reason
Farmed Fresh Atlantic Salmon has potential to be contaminated with Listeria monocytogenes.
Published
October 16, 2019
Distribution
Farmed Atlantic Salmon was sent to two c…

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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

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FDA Recall Ongoing Historical recordClass II

Losartan Potassium /Hydrochlorothiazide Tablets, USP 50mg/12.5mg, 90 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-116-90

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

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FDA Recall Ongoing Historical recordClass II

Losartan Potassium Tablets, USP 100 mg, [90 or 1000] tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC 90 tablets: 13668-115-90; NDC 1000 tablets: 13668-115-10

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

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FDA Recall Ongoing Historical recordClass II

Losartan Potassium Tablets, USP 50mg, 1000 tablets per bottle, Rx Only, Manufactured for: Torrent Pharma Inc., Basking Ridge, NJ 07920. NDC: 13668-409-10

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

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FDA Recall Terminated Historical recordClass II

Vivitrol (naltrexone for extended-release injectable suspension) 380 mg/vial. Each Carton Contains: 1) One vial of 380 mg of Vivitrol, 2) One vial containing 4 mL of diluent, 3) One 5-mL prepackaged syringe, 4) One 20-gauge 1-inch needle, 5) Two 20-gauge 1.5-inch safety needles, 6) Two 20-gauge 2-inch safety needles. Rx Only. Manufactured and marketed by: Alkermes, Inc. Kit NDC: 65757-300-01

by Alkermes, Inc.

Reason
Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch needles being placed in the 1 1/2 inch needle cardboard sleeve labelled as administration needles. The product vial is not impacted.
Published
October 9, 2019
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.