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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

State: RI ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 9, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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

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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

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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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Data last updated: September 9, 2026 ET

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.