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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 14,301–14,320 of 21,142 recalls

FDA Recall Terminated Historical recordClass III

Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15), b) 30 g tubes (NDC 0713-0638-31), and c) 90 g tubes (NDC 0713-0638-18), Rx only, Manufactured by: G&W Laboratories, Inc., South Plainfeld, NJ 07080.

by G & W Laboratories, Inc.

Reason
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749601

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749501

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 5242749401

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Almatica Pharma Inc. Pine Brook, NJ 07058 USA, NDC 50419-70305

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 90 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-370-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 60 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-369-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets, 60 mg, 100- count bottles, Rx only Manufactured for Almatica, Almatica Pharma Inc. Pinebrook, NJ 07058 USA, NDC 50419-702-05

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Adalat CC (nifedipine) Extended Release Tablets 30 mg, 100-count bottles, Rx only, Manufactured for Bayer Healthcare Bayer Healthcare Pharmaceuticals Inc. Whippany, NJ 07901 Manufactured in Germany, NDC 50419-701-05

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Nifedipine Extended-Release Tablets, 30 mg, 100-count bottles, Rx Only, Manufactured for Alvogen Inc. Pine Brook, NJ 07058 USA, NDC 47781-368-01.

by Alvogen, Inc

Reason
Cross Contamination with another product:residual powder found in inlet air duct identified as sorafenib
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 22709, NDC 0173-0682-20.

by GlaxoSmithKline, LLC

Reason
Defective Delivery System: Elevated number of units with out of specification results for leak rate.
Published
April 12, 2017
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Kalbitor (ecallantide), 10mg/mL, packaged in 3 vials per Carton, Rx Only, Dynax Corp., Burlington, MA. NDC47783-101-01

by Shire

Reason
Presence of Particulate Matter: Glass
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ;…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD N¿T Milk Chocolate with Hazelnut, 3.5 oz. (100g), UPC: 120293926000: the manufacturing process adds the undeclared ingredient almond to the product. The labeling carries a "May Contain" statement identifying Almond.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Choklad Ljus Milk Chocolate Net Wt 3.5 OZ; IKEA Produce…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD LJUS Milk Chocolate Bar, 3.5 oz. (100g), UPC: 1402939250003; the manufacturing process adds the undeclared ingredients Hazelnut and Almond . The labeling carries a "May Contain" statement identifying almond and hazelnuts.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Godis Chokladran Wafers filled and covered with Milk chocol…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. GODIS CHOKLADRAN Wafer Filled and Covered with Chocolate, 5.9 oz. (168g), UPC: 1202290300009, the ingredient statement fails to declare Hazelnut and Almond. The manufacturer's process adds hazelnut and almond to the product. The product labeling does include a "May Contains" statement identifying "tree nuts". This statement does not declare the almond and hazelnut.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Godis Chokladkrokant Milk chocolate with butterscotch pieces…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. GODIS CHOKLADKROKANT Milk Chocolate with Butterscotch, 15.9 oz. (450g); UPC: 1202155040002, as manufactured was found to contain undeclared ingredients: Hazelnut, Almond. Labeling does include a "May Contain" statement identifying: Almonds and Hazelnuts.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Choklad Lingon & Blabar Assortment of milk chocolate Squares…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD LINGON & BLABAR, 6.3 0z (180g), UPC: 1602184210009. Due to manufacturing process, the product contains the undeclared ingredients Hazelnut and Almond. The labeling carries a "May Contain" statement identifying Almonds and Hazelnuts.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

View recall →

FDA Recall United States Terminated Historical recordClass II

Ikea North America Srvcs Inc

Product
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.…
Reason
IKEA N.A. Services, LLC Voluntarily Issues Expanded Recall and Allergy Alert on Undeclared Milk, Almond, and/or Hazelnut on Certain IKEA Chocolate Products. CHOKLAD MORK, CHOKLAD MORK 70%, CHOKLAD LINGON & BLABAR, CHOKLAD NOT, GODIS CHOKLADKROKANT, GODIS CHOKLADRAN and CHOKLAD LJUS, are being recalled due to undeclared Milk, Hazelnuts and/or Almond. All Best Before Dates, Sold from April 30, 2015 to July 1, 2016. CHOKLAD MORK Dark Chocolate Bar, 3.5 oz. (100g), UPC: 1002939270003. Product has a may contain qualifying statement for milk, Almond and Hazelnut. The manufacturer's process adds Milk, Almond, Hazelnut to the chocolate but the label fails to declare milk, almond and hazelnut as ingredients. CHOKLAD MORK 70% Dark Chocolate Bars, 3.5 0z. (100g), UPC: 1203080940009, Contains: Milk, Almond, Hazelnut as ingredients. However, these allergens are declared in a "may contain statement" identifying the allergens as Milk and Treenuts.
Published
April 12, 2017
Distribution
AZ CA Co CT FL GA IL KS MA MD…

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FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

Product
artisanal cheese VULTO Creamery HANDMADE CHEESE, Walton Umbe…
Reason
Listeria monocytogenes contamination
Published
April 12, 2017
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

Product
artisanal cheese VULTO Creamery HANDMADE CHEESE, Hamden, NET…
Reason
Listeria monocytogenes contamination
Published
April 12, 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.