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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.

37,063
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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 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 2,181–2,200 of 21,105 recalls

FDA Recall Ongoing Historical recordClass II

Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT Rx, Dawsonville, GA 30534, Mfg By: Dr. Reddy's Laboratories LA, LLC, Shreveport, LA 71106, a) NDC 61919-0621-15 (15 count bottles), b) NDC 61919-0621-30 (30 count bottles, c) NDC 61919-0621-40 (40 count bottles), d) NDC 61919-0621-60 (60 count bottles), e) NDC 61919-0621-90 (90 count bottles), f) NDC: 61919-0621-100 and NDC: 61919-0621-71 (100 count bottles), g) NDC 61919-0621-72 (120 count bottles).

by Direct Rx

Reason
Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317

by Staska Pharmaceuticals, Inc.

Reason
Presence of Particulate Matter: Presence of glass particulates.
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL), 5mL Single-Dose Pre-filled Syringe, Rx only, Manufactured by: Baxter Pharmaceutical Solutions, LLC, Bloomington, IN 47403; Manufactured for: Baxter Healthcare Corporation, Deerfield, IL 60015. NDC: 36000-364-01

by Baxter Healthcare Corporation

Reason
Labeling: Missing Label
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Dapsone Gel 7.5%, 60 gram pump, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-094-02.

by VIONA PHARMACEUTICALS INC

Reason
Crystallization
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Morphine Sulfate Extended-Release Tablets 30 mg, 100-count bottles, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-186-01.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Impurities/Degradation Specification
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-185-01.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Impurities/Degradation Specification
Published
November 13, 2024
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

My Chai Inc

Product
Oregon Orchards Banana Smoothie Mix. Product is packaged in…
Reason
Acidified 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
MySyrup Sugar Free Salted Caramel Syrup. Product is packaged…
Reason
Acidified 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
MySyrup Sugar Free Raspberry Syrup. Product is packaged in…
Reason
Acidified 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
MySyrup Sugar Free Peppermint Syrup. Product is packaged in…
Reason
Acidified 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
MySyrup Sugar Free Madagascar Vanilla Syrup. Product is pack…
Reason
Acidified 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
MySyrup Sugar Free Hazelnut Syrup. Product is packaged in th…
Reason
Acidified 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
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

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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

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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

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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 →

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.