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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.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 3,021–3,040 of 21,188 recalls

FDA Recall OngoingHistorical recordClass I

LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-5

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

EQUATE brand Hydration PF Lubricant Eye Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.34 FL OZ (10 mL) bottles, Distributed by: Walmart Inc., Bentonville, AR 72712, NDC 79903-168-01

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Velocity Pharma brand Lubricating Eye Drop (Propylene glycol Eye Drops 0.6%), packaged in 3 bottles of 0.33 FL OZ (10 mL) each, Velocity Pharma, NDC 76168-502-30

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

Leader brand Lubricant Eye Drops (Propylene glycol Eye Drops 0.6%), packaged in 0.33 FL OZ (10 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0587-1

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Target brand High Performance Lubricant Eye Drops (Polyethylene glycol 400 0.4%, Propylene glycol 0.3%) a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 11673-522-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 11673-522-30), Distributed by: Target Corporation Minneapolis, MN 55403

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Leader brand Dry Eye Relief (Carboxymethylcellulose Sodium 1%), packaged in 0.5 FL OZ (15 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0089-1

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

CVS Health brand, Lubricant Gel Drops (Carboxymethylcellulose Sodium 1%) packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-704-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-704-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Leader brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline 0.05%), packaged in 0.5 FL OZ (15 mL) bottles, Cardinal Health Dublin, Ohio 43017, NDC 70000-0087-1

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass I

CVS brand Multi Action Relief Drops (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline 0.05%) packaged in 0.5 FL OZ (15mL) bottles, Distributed by CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-706-15

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Leader brand Dry Eye Relief (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%) packaged in 0.33 FL OZ (10 mL) bottles, Distributed by Cardinal Health Dublin, Ohio 43017, NDC 70000-0088-1

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricating Gel Drops (Polyethylene glycol 400 0.4% and Propylene glycol 0.3%), packaged in 0.33 FL OZ (10 mL) bottles, Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895. NDC 76168-712-10

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Rugby brand Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15 mL) bottles, Distributed by: Rugby Laboratories, Livonia, MI 48152, NDC 0536-1325-94

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricant Eye Drops (Propylene glycol 0.6%), packaged in a) 0.33 FL OZ (10mL) bottles (Single Pack) (NDC 76168-714-10) and b) 0.33 FL OZ (10 mL) bottles (Twin pack) (NDC 76168-714-20), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Leader brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 70000-0090-1) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 70000-0090-2), Distributed by: Cardinal Health Dublin, Ohio 43017

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

CVS Health brand Lubricant Eye Drops (Carboxymethylcellulose Sodium 0.5%), packaged in a) 0.5 FL OZ (15mL) bottles (Single Pack) (NDC 76168-702-15) and b) 0.5 FL OZ (15 mL) bottles (Twin pack) (NDC 76168-702-30), Distributed by: CVS Pharmacy Inc. One CVS Drive Woonsocket, RI 02895.

by Kilitch Healthcare India Limited

Reason
Non-Sterility
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 17, 2024Historical recordClass II

Omeza Skin Protectant, Skin Protectant Gel 10*2mL Vials

by OMEZA LLC

Reason
CGMP Deviations
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: October 17, 2024Historical recordClass II

Omeza Lidocaine Lavage pain relief oil 10*2mL VIALS

by OMEZA LLC

Reason
CGMP Deviations
Published
February 14, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: December 16, 2025Historical recordClass III

NOW Foods

Product
Protocol for Life Balance, Phosphatidyl Serine 300mg softgel…
Reason
Amount of Phosphatidyl Serine in product is less than stated on the label
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 1, 2024Historical recordClass II

County Fair Foods, Inc.

Product
Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to…
Reason
Undeclared Yellow #5
Published
February 14, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 18, 2024Historical recordClass I

Zenzedi (Dextroamphetamine Sulfate) CII Tablets, USP, 30 mg, 30-count bottle, Rx only, Mfd. for: Arbor Pharmaceuticals, LLC., Atlanta, Georgia, 30328, NDC 24338-856-03

by Azurity Pharmaceuticals, Inc.

Reason
Labeling: Label Mix-up
Published
February 7, 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.

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