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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
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 12,281–12,300 of 22,149 recalls

FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, 100-count bottoles, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141 Manufactured by: Sandoz Inc. Princeton, NJ 08540,NDC 16714-439-01

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Isosorbide Dinitrate Tablets, USP 20 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-222-00

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Isosorbide Dinitrate Tablets, USP 10 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-225-00

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Isosorbide Dinitrate Tablets, USP 5 mg,100-count bottles, Rx Only Manufactured by: Sandoz Inc., Princeton, NJ 08540 For BluePoint Laboratories, NDC 68001-223-00

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Isosorbide Dinitrate Tablets, USP 20 mg, 100-count bottles, Rx Only, Distributed by: Sandoz Inc. Princeton, NJ 08540; NDC 0781-1695-01

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals) 100 mg, packaged in a) 100-capsule bottles (NDC 0185-0122-01); and b) 1000-capsule bottles, (NDC 0185-0122-10); Rx Only, Distributed by Sandoz Inc. Princeton, NJ 08540

by Sandoz Inc

Reason
Cross Contamination with Other Products
Published
November 21, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

puriton EYE RELIEF DROPS, 0.5 oz (15 ml) bottle, Kadesh Inc., NDC#7079600115, UPC 7 36972 16799 0.

by Kadesh International

Reason
Non-Sterility: Product manufactured under non-sterile production conditions.
Published
November 21, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro Sanitario No SD2014-0002208 LLC-USA

by Zero Xtreme USA

Reason
Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine
Published
November 21, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Sirob Imports, Inc.

Product
FC Finest Choice Hot Curry Powder, Packed By SIROB IMPORTS,…
Reason
Products may contain elevated levels of lead.
Published
November 21, 2018
Distribution
Multiple states

View recall →

FDA Recall United States Terminated Historical recordClass I

Sirob Imports, Inc.

Product
Curry powder packaged under bulk, retail, and food service l…
Reason
Products may contain elevated levels of lead.
Published
November 21, 2018
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Simply Fresh Foods, Inc

Product
Rojo's Autentico Black Bean 5 Layer Dip; Layers of Black Be…
Reason
Firm was notified by McCain Foods that the corn used in their layer dip is being recalled due to potential Salmonella/Listeria monocytogenes contamination.
Published
November 21, 2018
Distribution
One distributor - locations in PA, MO, N…

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FDA Recall United States Terminated Historical recordClass II

Deli Star Ventures Inc. dba King's Food Products

Product
Chef s Request professional steak marinade and Buckhead wil…
Reason
Deli Star Inc. dba King's Food Products initiated a voluntary recall of Chef s Request professional steak marinade and Buckhead wildlife marinade due to undeclared allergens soy and wheat.
Published
November 21, 2018
Distribution
Domestic: Illinois Foreign/VA/DOD: No…

View recall →

FDA Recall United States Terminated Historical recordClass II

The Wornick Company

Product
Chef Sensations Fire Roasted 1/2" diced onion/pepper blend N…
Reason
Firm received notification from their supplier of a voluntary recall due to the potential contamination of Salmonella and/or Listeria.
Published
November 21, 2018
Distribution
All consignees are CONUS and OCONUS mili…

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FDA Recall Terminated Historical recordClass II

Healthful Naturals Leg Cramp Support Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906 NDC 68703-206-02

by Silver Star Brands

Reason
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published
November 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Healthful Naturals DizziFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-204-02

by Silver Star Brands

Reason
CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.
Published
November 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Native Remedies EyeClear Pro Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-151-59

by Silver Star Brands

Reason
Microbial Contamination of Non-Sterile Product
Published
November 14, 2018
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Native Remedies HypoSlim Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-275-02

by Silver Star Brands

Reason
Microbial Contamination of Non-Sterile Products
Published
November 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Native Remedies VertiFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-253-02

by Silver Star Brands

Reason
Microbial Contamination of Non-Sterile Products
Published
November 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

SparkleFresh Fluoride Toothpaste, Sodium Monofluorophosphate 0.76%, a) 17 g tube (NDC 53329-083-92, product number NONTP6I), b) 24 g tube (NDC 53329-083-93, product number NONTP85I), c) 42.5 g (NDC 53329-083-21, product number NONTP15I), d) 24 g tube (NDC 53329-081-93, product number DGN1000), Made in Malaysia for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60093 USA

by Medline Industries Inc

Reason
Microbial Contamination of Non-Sterile Product
Published
November 14, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) vials, Rx Only Qualgen, LLC, Edmond, OK 73013

by Qualgen, LLC

Reason
Lack of Assurance of Sterility
Published
November 14, 2018
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.