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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.

37,061
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 recallhttps://www.fsis.usda.gov/recalls-alerts/el-eden-import-distributor-corp-recalls-ineligible-pork-cracklings-products-importedPublished September 9, 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 II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 1,501–1,520 of 20,201 recalls

FDA Recall Ongoing Historical recordClass II

Cephalexin for Oral Suspension, USP, 125 mg per 5 mL, 100 mL (when mixed), Rx Only, Manufactured by: Alkem Laboratories Ltd., India, Distributed by: Ascent Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-544-88

by Ascend Laboratories, LLC

Reason
Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.

by SAINI TRADE INC

Reason
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Ezetimibe and Simvastatin Tablets, 10mg/40mg, 90-count bottle, Rx only, Manufactured by: Glenmark Pharmaceuticals Ltd., Plot No. 2, Phase-2, Pharma Zone SEZ, Madya Pradesh, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-323-90

by Glenmark Pharmaceuticals Inc., USA

Reason
Failed Impurities/Degradation Specifications: Out of Specification (OOS) for related substances test for Anhydro Simvastatin at the 06-month time point during long-term stability study.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Chlorthalidone Tablets, USP, 25 mg, 50 Tablets (5x10) Unit Dose cards per carton, Rx only, Manufactured for: AvKARE, Pulaski, TN 38478, NDC 50268-167-15

by AvKARE

Reason
Failed Dissolution Specifications
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 50268-169-15

by AvKARE

Reason
Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was found in 500 count bottle of Celecoxib 200 mg capsules
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71

by Alembic Pharmaceuticals Limited

Reason
Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sealed 500-count bottle of Celecoxib 200mg capsule
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

GBC Food Services, LLC

Product
Supreme Produce Apple & PB Snack Cup. Net Wt: 8oz (226g).…
Reason
Foreign Material (plastic)
Published
June 18, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

GBC Food Services, LLC

Product
Supreme Produce Celery & PB Snack Cup. Net Wt: 9oz (225g).…
Reason
Foreign Material (plastic)
Published
June 18, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonvil…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
PR Cucumber Sliced 2/5# 1/4 Pack Date May 22 Product of USA…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber 5lb Repacked by Lipman Produce Hendersonville, NC 2…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonvil…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass I

LIPMAN FAMILY FARMS

Product
Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC…
Reason
Potential Salmonella Contamination
Published
June 18, 2025
Distribution
Product was distributed to AZ, CA, IL, F…

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FDA Recall United States Terminated Historical recordClass III

NOW Foods

Product
NOW Nutritional Yeast Powder, Nt. Wt. 10oz. UPC 7 33739 024…
Reason
regular yeast was inadvertently packaged as nutritional yeast
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product
Instant Milk Tea Original Flavor, R&M Refresher brand, B0D71…
Reason
The Instant Milk Tea Powder's ingredients statement declares Non-Dairy Creamer (Whey Powder, Sodium Caseinate) but does not specify milk.
Published
June 18, 2025
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.