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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to November 2026.

37,449
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,872
Class I recallsReasonable probability of serious health consequences
24,509
Class II recallsTemporary or medically reversible health consequences
2,932
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 2,096 recalls
Most affected stateHawaii 200 recalls mention this state

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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)

  • 1,956 recalls have been announced year to date.
  • Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
  • Nov 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 II24,509
Class I9,872
Class III2,932
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,509
Class I9,872
Class III2,932
Not Yet Classified2

Showing 8,361–8,380 of 21,307 recalls

FDA Recall TerminatedTerminated: November 2, 2021Historical recordClass III

Testosterone Cypionate Injection, USP CIII 200mg/ml FOR INTRAMUSCULAR USE ONLY 1mL Single-dose vial Distributed by: Sun Pharma Ind. Inc, NJ 08512 Manufactured by: Sun Pharma Ind. Ltd., India NDC 62756-015-40

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Incorrect Labeling: Incorrect lot number on secondary packaging
Published
February 3, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2023Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 10.1 fl. oz. (300 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as Thrifty White Pharmacy Wash-Free Hand Sanitizer. UPC 8 19845 00599 2

by Shane Erickson Inc

Reason
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published
February 3, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2023Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 3.4 fl. oz. (100 ml), Made in China, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384. Labeled as a) SAFE-GUARD Products International, b) Safe-WAY JEVCO Wash-Free Hand Sanitizer, c) TRACTION CAPITAL, d) United States Census 2020. UPC 8 19845 00598 5

by Shane Erickson Inc

Reason
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published
February 3, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 29, 2023Historical recordClass II

IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) bottles, Distributed by IMC 4284 Shoreline Dr, Spring Park, MN 55384, Made in China, ALSO distributed with Custom front labels as follows a) Sadie G. Mays Health & Rehabilitation Center, b) Pacers logo, c) northwood CHURCH, d) ROGERTHEROOFER.com and e) SoFi Stadium Wash-Free Hand Sanitizer. UPC 8 19845 00597 8

by Shane Erickson Inc

Reason
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Published
February 3, 2021
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 12, 2021Historical recordClass II

EMILIA FOODS SRL

Product
Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Ke…
Reason
Good and Gather Four Cheese Gnocchi may contain foreign material.
Published
February 3, 2021
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: March 19, 2021Historical recordClass II

Nueske Applewood Smoked Meat, Inc

Product
Cinnamon Walnut Coffee Cake, Item 258, Net Wt. 24 oz.
Reason
Coffee cake may contain undeclared wheat, egg, milk, and walnuts.
Published
February 3, 2021
Distribution
AR, CA, CO, CT, IA, IL, IN, KY, MD, MI,…

View recall →

FDA Recall United States TerminatedTerminated: March 19, 2021Historical recordClass II

Nueske Applewood Smoked Meat, Inc

Product
Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.
Reason
Coffee cake may contain undeclared wheat, egg, and milk.
Published
February 3, 2021
Distribution
AR, CA, CO, CT, IA, IL, IN, KY, MD, MI,…

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FDA Recall United States TerminatedTerminated: June 15, 2021Historical recordClass II

Samyang Foods Co Ltd

Product
Samyang Buldak Hot Chicken Flavor Sauce Hot Chili Sauce Ne…
Reason
Undeclared allergens of egg, milk, and wheat
Published
February 3, 2021
Distribution
Multiple states

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FDA Recall United States TerminatedTerminated: June 15, 2021Historical recordClass II

Samyang Foods Co Ltd

Product
Samyang Buldak Carbonara Hot Chicken Flavor Sauce Hot Chili…
Reason
Undeclared wheat, egg, and coconut oil
Published
February 3, 2021
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: June 15, 2021Historical recordClass II

Samyang Foods Co Ltd

Product
Samyang Buldak Extremely Spicy Hot Chicken Flavor Sauce Hot…
Reason
Undeclared allergens of egg, milk, and wheat
Published
February 3, 2021
Distribution
Multiple states

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

Weis Markets, Inc., Ice Cream Division

Product
Nelsons Graham Slam Bulk. Packaged in a 3 gallon paper drum.
Reason
Ice Cream product may contain metal (foreign objects).
Published
February 3, 2021
Distribution
Distributed to warehouse in PA and retai…

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FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

Weis Markets, Inc., Ice Cream Division

Product
Klein s Cookies and Cream Bulk Packaged in a 3 gallon paper…
Reason
Ice Cream product may contain metal (foreign objects).
Published
February 3, 2021
Distribution
Distributed to warehouse in PA and retai…

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FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

Weis Markets, Inc., Ice Cream Division

Product
Klein s Vanilla Ice Cream. Packaged in a 3 gallon paper drum…
Reason
Ice Cream product may contain metal (foreign objects).
Published
February 3, 2021
Distribution
Distributed to warehouse in PA and retai…

View recall →

FDA Recall United States TerminatedTerminated: February 15, 2022Historical recordClass II

Weis Markets, Inc., Ice Cream Division

Product
Weis Quality Cookies and Cream Ice Cream (48oz). Packaged i…
Reason
Ice Cream product may contain metal (foreign objects).
Published
February 3, 2021
Distribution
Distributed to warehouse in PA and retai…

View recall →

FDA Recall TerminatedTerminated: June 7, 2023Historical recordClass II

Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free 11.25mg / 0.5ml (22.5mg/ml) 0.5ml per syringe. KEEP FROZEN UNTIL USE AND PROTECT FROM LIGHT SINGLE USE SYRINGE FOR INTRAOCULAR INJECTION Edge Pharma, LLC is an FDA-registered 503B outsourcing facility. This is a compounded (re-packaged) drug. Not for Resale, Hospital/Office use only. Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 Customer Service (USA) 1-802-992-1178

by Edge Pharma, LLC

Reason
Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.
Published
January 27, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason
CGMP deviations: Lack of potency testing.
Published
January 27, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 5,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason
CGMP deviations: Lack of potency testing.
Published
January 27, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 6,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason
CGMP deviations: Lack of potency testing.
Published
January 27, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: September 28, 2022Historical recordClass II

HUMAN CHORIONIC GONADOTROPIN 11,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in water for injection. Lyophilized, Unpreserved. Complete Pharmacy & Medical Solutions 5829 NW 158th St, Miami Lakes, FL 33014 Tel: 305-397-2035

by Complete Pharmacy and Medical Solutions, LLC.

Reason
CGMP deviations: Lack of potency testing.
Published
January 27, 2021
Distribution
Nationwide

View recall →

FDA Recall TerminatedTerminated: June 21, 2023Historical recordClass II

Refresh Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz (10 mL) Sterile Distributed by: Allergan, an AbbVie company Madison, NJ 07940 UPC 3 00236 63410 0, NDC 0023-6634-10.

by Allergan, PLC.

Reason
Labeling: Missing instructions for use insert
Published
January 27, 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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