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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.

37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,761–5,780 of 17,229 recalls

FDA Recall Terminated Historical recordClass III

DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, 5000 mL bags, 2-pack, Rx Only, Fresenius Medical Care NA, Waltham, MA 02451, NDC 49230-0188-50

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Chloride 0.9%, USP, 1000 mL, Mfg by: Fresenius Medical Care North America, Waltham, MA 02451, NDC 46163-0300-10

by Fresenius Medical Care Holdings, Inc.

Reason
Temperature Abuse: Product exposed to temperature outside specified limits.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Arizona Nutritional Supplements

Product
365 Everyday Value Whey Protein Powder Natural Vanilla Flavo…
Reason
Whey Protein Powder was mistakenly packaged with Soy Protein Powder.
Published
June 16, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

1% Lidocaine HCl Injection, USP, 300 mg/30 mL (10 mg/mL), 30 mL Single-dose vial (NDC 0409-4279-16), packaged in 25 vials per tray (NDC 0409-4279-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason
Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC 0409-1162-19), packaged in 25 vials per tray (NDC 0409-1162-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason
Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published
June 9, 2021
Distribution
Nationwide

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FDA Recall Completed Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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

View recall →

FDA Recall United States Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Ongoing Historical 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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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.