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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.

37,137
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 11,521–11,540 of 17,335 recalls

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

View recall →

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 I

Vulto Creamery

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

View recall →

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 →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

Product
artisanal cheese VULTO Creamery HANDMADE CHEESE, Blue Blais
Reason
Listeria monocytogenes contamination
Published
April 12, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

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

View recall →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

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

View recall →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

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

View recall →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

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

View recall →

FDA Recall United States Terminated Historical recordClass I

Vulto Creamery

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

View recall →

FDA Recall Terminated Historical recordClass III

Montelukast sodium tablets, 10 mg, 30-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, By: HETERO Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-726-30

by Hetero USA Inc

Reason
Discoloration: the firm received a complaint of a sealed bottle in which tablets inside had blue spots and a blue powder inside the bottle.
Published
April 5, 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.