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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.

37,060
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,786
Class I recallsReasonable probability of serious health consequences
24,313
Class II recallsTemporary or medically reversible health consequences
2,876
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026
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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,861–1,880 of 17,993 recalls

FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MySyrup Sugar Free Coconut Syrup. Product is packaged in the…
Reason
Acidified product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MySyrup Sugar Free Caramel Syrup. Product is packaged in the…
Reason
Acidified product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MySyrup Sugar Free Almond Syrup. Product is packaged in the…
Reason
Acidified product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MyChai Chai Tea Concentrate Original Double. Product is pack…
Reason
Acidified Chai Tea product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MyChai Chai Tea Concentrate Super. Product is packaged in th…
Reason
Acidified Chai Tea product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
MyChai Chai Tea Concentrate Double. Product is packaged in t…
Reason
Acidified Chai Tea product is recalled due to lack production record.
Published
November 13, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass II

My Chai Inc

Product
MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is pack…
Reason
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

My Chai Inc

Product
MyChai Chai Tea Concentrate Original. Product is packaged in…
Reason
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Published
November 13, 2024
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

Hammond's Candies Since 1920 II, LLC

Product
Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged…
Reason
Undeclared allergen: milk
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 90 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-442-10, b) 90 Tablets per bottle, NDC: 16729-442-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.

by ACCORD HEALTHCARE, INC.

Reason
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 60 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-441-10, b) 90 Tablets per bottle, NDC: 16729-441-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.

by ACCORD HEALTHCARE, INC.

Reason
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets 30 mg, Rx Only, a) 30 Tablets per bottle, NDC: 16729-440-10, b) 90 Tablets per bottle, NDC: 16729-440-15, Manufactured for: Accord Healthcare, Inc., Durham, NC 27703, Manufactured by: Intas Pharmaceuticals Limited, Ahmedabad - 382 210, INDIA.

by ACCORD HEALTHCARE, INC.

Reason
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 90 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India., NDC 43598-369-30.

by Dr. Reddy's Laboratories, Inc.

Reason
CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 60 mg, 30-count bottles, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-368-30.

by Dr. Reddy's Laboratories, Inc.

Reason
CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Cinacalcet Tablets, 30 mg, 30-count bottle, Rx Only, Dr. Reddy's Laboratories Inc, Princeton, NJ 08540, Made in India, NDC 43598-367-30.

by Dr. Reddy's Laboratories, Inc.

Reason
CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit
Published
November 6, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06.

by Akron Pharma, Inc.

Reason
CGMP Deviations
Published
October 30, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas, 400 mg,

by C & A Naturistics

Reason
Marketed without an Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared diclofenac and acetaminophen.
Published
October 30, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Thiamine HCl 0.9% Sodium Chloride Injection USP, 500 mg per 100 mL, Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-079-56

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

EPINEPHrine 0.9% Sodium Chloride Injection USP, 8 mg per 250 mL Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-060-58

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 0.9% Sodium Chloride Injection USP, 30 units per 500 mL Single Dose Bag, Rx only, Fagron Sterile Services, Canton, MA NDC: 71506-028-59

by Fresenius Kabi Compounding, LLC

Reason
cGMP violations
Published
October 30, 2024
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.