Skip to main content
Get Alerts

Data Explorer

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 November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026
Most affected stateHawaii 200 recalls mention this state

Advertisement

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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 7,601–7,620 of 21,307 recalls

FDA Recall United States TerminatedTerminated: August 23, 2022Historical recordClass I

Simply Delicious, Inc.

Product
Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack,…
Reason
Almond Butter Bars contain undeclared peanuts.
Published
November 17, 2021
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: August 12, 2024Historical recordClass III

NOW Health Group Inc.

Product
NOW Bee Pollen 500mg 100 VCAPS UPC 733739025203
Reason
Product may contain Metronidazole
Published
November 17, 2021
Distribution
Total number of domestic consignees = 15…

View recall →

FDA Recall United States TerminatedTerminated: August 12, 2024Historical recordClass III

NOW Health Group Inc.

Product
NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutr…
Reason
Product may contain Metronidazole
Published
November 17, 2021
Distribution
Total number of domestic consignees = 15…

View recall →

FDA Recall United States TerminatedTerminated: August 12, 2024Historical recordClass III

NOW Health Group Inc.

Product
NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal…
Reason
Product may contain Metronidazole
Published
November 17, 2021
Distribution
Total number of domestic consignees = 15…

View recall →

FDA Recall United States TerminatedTerminated: June 9, 2023Historical recordClass I

Best Foods NJ, Inc.

Product
Sundelight Golden Raisins Net Wt 7oz. UPC: 14760 84059. Plas…
Reason
Undeclared sulfites
Published
November 17, 2021
Distribution
Distributed to retail stores in MD, NJ,…

View recall →

FDA Recall TerminatedTerminated: July 25, 2023Historical recordClass I

Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01

by MERCK SHARP & DOHME CORP

Reason
Presence of Particulate Matter: Identified as Glass Particles
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass I

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Reason
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 30, 2023Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 30, 2023Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 30, 2023Historical recordClass II

Irbesartan Tablets USP, 300 mg a) 30 count (NDC 68180-412-06) and b) 90 count NDC# 68180-412-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 30, 2023Historical recordClass II

Irbesartan Tablets USP, 150 mg a) 30 count (NDC 68180-411-06) and b) 90 count (NDC 68180-411-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: January 30, 2023Historical recordClass II

Irbesartan Tablets USP, 75 mg a) 30 count (NDC 68180-410-06) and b) 90 count (NDC 68180-410-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 count bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA NDC 43598-743-05

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin Tablets, 10 mg/10 mg were found in the bottle
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 count (NDC 43598-743-30), b) 90 count (NDC 43598-743-90) bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/80 mg, a) 30 count (NDC 43598-745-30), b) 90 count (NDC 43598-745-90), and c) 500 count (NDC 43598-745-05) bottles, Rx Only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 count (NDC 43598-744-30), b) 90 count (NDC 43598-744-90) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass II

Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 count (NDC 43598-742-90) and b) 1000 count (NDC 43598-742-10) bottles, Rx only, Manufactured by: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106, USA, Distributed by: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540 USA, , packaged in bottles.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Published
November 10, 2021
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: September 9, 2022Historical recordClass I

Cedar's Mediterranean Foods, Inc.

Product
Cedar s Organic Mediterranean Hommus 10 oz.
Reason
May contain undeclared tree nuts (pine nuts)
Published
November 10, 2021
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: February 18, 2022Historical recordClass I

ProSource Produce LLC

Product
Whole raw WHITE onions are imported from Chihuahua of MEXICO…
Reason
Salmonella Oranienburg.
Published
November 10, 2021
Distribution
Distributed in AL, AR, AZ, CA, CO, CT, F…

View recall →

FDA Recall United States TerminatedTerminated: February 18, 2022Historical recordClass I

ProSource Produce LLC

Product
Whole raw YELLOW onions are imported from Chihuahua of MEXIC…
Reason
Salmonella Oranienburg.
Published
November 10, 2021
Distribution
Distributed in AL, AR, AZ, CA, CO, CT, F…

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.

Reconnecting to the server…

We lost the connection to the server.

Your session has expired.