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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 October 2026.

37,326
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,859
Class I recallsReasonable probability of serious health consequences
24,440
Class II recallsTemporary or medically reversible health consequences
2,900
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 2,095 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,440
Class I9,859
Class III2,900
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,440
Class I9,859
Class III2,900
Not Yet Classified2

Showing 5,861–5,880 of 17,324 recalls

FDA Recall CompletedHistorical recordClass II

BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle, Rx only, Manufactured By: Oxford Pharmaceuticals, LLC Birmingham, Alabama 35211, NDC 69584-093-10

by Oxford Pharmaceuticals, LLC

Reason
Presence of Foreign Tablets/Capsules
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 18, 2022Historical recordClass III

Thiamine HCl Injection, USP 200 mg/2 mL (100mg/mL), 2 mL vials, packaged in 25 (2 mL multi-dose vial) per carton, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA; Manufactured by: Mylan Institutional, Galway, Ireland. NDC: 67457-196-02

by Mylan Institutional LLC

Reason
Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct lot number 200906 contain vials labeled with the incorrect lot number 200901.
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Mixed Berry Low Sugar Bar 50g x 10 Clio Reta…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Raspberry / Peach Mini Club pack Clio 24g x…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Greek Yogurt Bar Strawberry Minis 6.2oz pouch x 6 pouch…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Coconut Less Sugar Bar 45g x 10 Clio Retail…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Berry Acai Less Sugar 45g x 10 Clio Retail…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Yogurt Bar Strawberry 50g x 10 Clio Retail 10-pack. UP…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Greek Yogurt Bar Honey 50g x 10 Clio Retail 10-pack. UP…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Greek Yogurt Bar Vanilla 50g x 10 Clio Retail 10-pack.…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio Greek Yogurt Bar Vanilla / Strawberry Club pack 50g x 1…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 14, 2022Historical recordClass II

Clio LLC

Product
Clio No Added Sugar Yogurt Bar Mixed Berry / Peach 50g x 16…
Reason
Possible metal fragments in Yogurt Bars
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 90 Thyroid Tablets, USP 1&1/2 grain (90 mg) 100-count bottles, Rx only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005, NDC 42192-331-01

by Acella Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 15 Thyroid Tablets, USP 1/4 grain (15 mg), packaged in a) 100-count bottles (NDC 42192-327-01) and b) 7-count bottles (NDC 42192-327-07), Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 15 mg over 9 hours (1.6 mg/hr), 30 Patches (NDC 68968-5553-1) per box (NDC 68968-5553-3), Rx only, Manufactured for Noven Therapeutics, LLC., Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186.

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: The number of customer complaints for ripping patches and tight release/adhesive transfer have exceeded the action limits.
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Daytrana (methylphenidate transdermal system), Delivers 10 mg over 9 hours (1.1 mg/hr), 30 Patches (NDC 68968-5552-1) per box (NDC 68968-5552-3), Rx only, Manufactured for Noven Therapeutics, LLC., Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186.

by Noven Pharmaceuticals Inc

Reason
Defective Delivery System: The number of customer complaints for ripping patches and tight release/adhesive transfer have exceeded the action limits.
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: February 16, 2023Historical recordClass III

Atorvastatin Calcium Tablets, USP 10 mg*, Rx Only, 500 count bottle, Mfd By: Dr. Reddy's Laboratories Limited, Bachupally 500 090, India, NDC 55111-121-05.

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Impurities -Degradation Specifications:due to presence of ATV cyclo IP and FP impurities
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 120 Thyroid Tablets, USP 2 grain (120 mg), packaged in a) 100-count bottles (NDC 42192-328-01) and b) 7-count bottles (NDC 42192-328-07) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 60 Thyroid Tablets, USP 1 grain (60 mg) 100-count bottles, Rx Only Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005, NDC 42192-330-01

by Acella Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
June 2, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: March 13, 2024Historical recordClass I

NP Thyroid 30 Thyroid Tablets, USP 1/2 grain (30 mg), packaged in a) 100-count bottles (NDC 42192-329-01) and b) 7-count bottles (NDC 42192-329-07), Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 30005

by Acella Pharmaceuticals, LLC

Reason
Subpotent Drug
Published
June 2, 2021
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.

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