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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.

37,118
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 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 10,661–10,680 of 17,327 recalls

FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 5 mL, 100 mg/5 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Succinylcholine Chloride Injection Solution 10 mL, 200 mg/10 mL (20 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-067-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 1 mL 0.2 mg/1 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 2 mL 0.4 mg/2 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-16

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Glycopyrrolate Injection Solution, 5 mL 1 mg/5 mL (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222; NDC 52533-028-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 50 mg/5 mL (10 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-118-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate Injection Solution 1 mL, 50 mg/1 mL (50 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-258-45

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 5 mL, 25 mg/5 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-15

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL, 50 mg/10 mL (5 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207 877-666-5222, NDC 52533-019-12

by Cantrell Drug Company

Reason
Lack of Sterility Assurance.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Nystatin Topical Powder, USP, 100,000 USP units per gram, 15 grams per bottle, Rx only, Vensun, NDC 42543-052-61

by X-Gen Pharmaceuticals Inc.

Reason
Presence of Foreign Substance: potential presence of plastic particles.
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass I

Garden Of Light Inc.

Product
WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC…
Reason
Potential for Listeria contamination
Published
August 16, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30

by PD-Rx Pharmaceuticals, Inc.

Reason
Failed Tablet/Capsule Specification: out of specification for tablet weight.
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

by Teva Pharmaceuticals USA

Reason
Failed Tablet/Capsule Specification; out of specification for tablet weight
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ibuprofen Tablets, USP 600 mg, 500-count bottle (Capsule Shaped), Rx only, Manufactured for: Time Cap Labs, Inc., 7 Michael Avenue Farmingdale, NJ 11735, USA, Manufactured by: Marksans Pharma Ltd. Plot No. L-82, L-83 Verna Indl. Estate, Verna, Goa-403 722, India, NDC 49483-603-50

by Time-Cap Laboratories, Inc.

Reason
Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles were found to contain some Ibuprofen Tablets USP 800 mg.
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085

by Bayer HealthCare Pharmaceuticals, Inc.

Reason
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048

by Bayer HealthCare Pharmaceuticals, Inc.

Reason
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194

by Bayer HealthCare Pharmaceuticals, Inc.

Reason
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 250 mg 100-count bottle (NDC 68382-032-01), b.) 500-count bottle (NDC 68382-032-05),Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications
Published
August 9, 2017
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054, NDC 68382-031-01

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications
Published
August 9, 2017
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.