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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

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

State: NE ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 6, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express Chopped Kit Chipotle Cheddar 11.4 oz, UPC 0712…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express Chopped Kit BBQ Ranch 11.3 oz, UPC 07127930907…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express Chopped Kit Bacon & Bleu 10.9 oz, UPC 07127930…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express Chopped Kit Asian 12 oz, UPC 071279302027, (C…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express America's Fresh 3 Color Deli Cole Slaw" 14 o…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express America's Fresh Old Fashioned Cole Slaw" 14oz,…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Signature Farms Garden Salad, 12 oz, UPC 021130981359, Iceb…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Fresh Express Iceberg Garden / Lechuga Repollo 24 oz., UPC 0…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall United States TerminatedTerminated: October 15, 2020Historical recordClass II

Garland Ventures, LTD DBA Bally Plus

Product: Freshness Guaranteed Five Cheese Stuffed Shells Traditional…
Reason: Potential contamination with Listeria monocytogenes
Published: July 22, 2020
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: December 16, 2020Historical recordClass II

Fresh Express Incorporated

Product: Little Salad Bar Garden, 12 oz, UPC 4099100082975, Iceberg l…
Reason: Ready to Eat salad products containing iceberg lettuce, red cabbage and/or carrot ingredients are recalled due to a possible health risk from Cyclospora.
Published: July 22, 2020
Distribution: Domestic: Midwestern states of AR, CT, D…

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FDA Recall TerminatedTerminated: March 11, 2022Historical recordClass II

Cetrotide (cetrorelix acetate for Injection) 0.25 mg, Sterile - for subcutaneous use only, Rx Only, Manufactured for: EMD Serono, Inc., Rockland, MD 02370, NDC: 44087-1225-1

by EMD Serono, Inc.

Reason: Defective Container: Market complaints of missing rubber stoppers from drug vial. Missing rubber stoppers could lead to lack of sterility assurance.
Published: July 15, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 30, 2023Historical recordClass III

Brimonidine Tartrate Opthalmic Solution 0.2%, 15 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India. NDC 70069-233-01

by SOMERSET THERAPEUTICS LLC

Reason: Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the shelf life.
Published: July 15, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 30, 2023Historical recordClass III

Brimonidine Tartrate Opthalmic Solution 0.2%, 10 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India. NDC 70069-232-01

by SOMERSET THERAPEUTICS LLC

Reason: Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the shelf life.
Published: July 15, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 30, 2023Historical recordClass III

Brimonidine Tartrate Opthalmic Solution 0.2%, 5 mL bottle, Rx only, Manufactured for: Somerset Therapeutics, LLC Hollywood, FL 33024. Made in India. NDC 70069-231-01

by SOMERSET THERAPEUTICS LLC

Reason: Failed Impurities/Degradation Specification: There is a slow leaching process from the product label on the bottle which may impact the product over the shelf life.
Published: July 15, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 3, 2020Historical recordClass III

Zilretta (triamcinolone acetonide extended-release injectable suspension), 32mg per vial, 5mL vials, Single-dose Kits, Rx Only, Manufactured for: Flexion Therapeutics, Inc. 10 Mall Road, Suite 301, Burlington, MA 01803, NDC 70801-003-01

by Flexion Therapeutics, Inc.

Reason: Temperature Abuse: Product was stored at room temperature longer than 6 weeks and was inadvertently distributed instead of discarded
Published: July 8, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2022Historical recordClass II

Childrens Dimetapp Cold & Cough, For ages 6 yrs. & over, 8 FL OZ. bottle, (237 mL), Distributed by: Pfizer Madison, NJ 07940, Made in Canada, UPC: 60300312234196, NDC: 0031-2234-19.

by Glaxosmithkline Consumer Healthcare Holdings

Reason: Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.
Published: July 8, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 3, 2022Historical recordClass II

Childrens Robitussin Honey Cough and Chest Congestion DM, dextromethorphan (cough suppressant), guaifenesin (expectorant), 4 FL OZ. bottle (118 mL), Distributed by: Pfizer, Madison, NJ 07940 USA, UPC: 50300318760128, NDC: 0031-8760-12.

by Glaxosmithkline Consumer Healthcare Holdings

Reason: Defective Delivery System: the dosing cups are missing graduations applicable to certain age groups.
Published: July 8, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 24, 2022Historical recordClass II

Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 100 Tablets (10 x 10) unit dose cartons, Rx only, Manufactured by: Apotex, Inc., Toronto, Ontario, Canada, Manufactured for: Apotex Corp. Weston, FL, Distributed by: Major Pharmaceuticals, Livonia, MI 48152 NDC 00904-5794-61

by The Harvard Drug Group

Reason: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity above the established levels.
Published: July 8, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 11, 2024Historical recordClass II

Koala Hand Sanitizer, Unscented, 16 FL OZ., Antibacterial, (Ethyl Alcohol 70%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665

by Beaming White Llc

Reason: Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Published: July 8, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: March 11, 2024Historical recordClass II

Koala Hand Sanitizer, Menthol, 16 FL OZ., Antibacterial, (Ethyl Alcohol 69%), Manufactured by Beaming White LLC, 1205 NE 95th St., Vancouver, WA 98665

by Beaming White Llc

Reason: Subpotent Drug: active ingredient ethanol tested below label claim and there is presence of undeclared isopropyl alcohol.
Published: July 8, 2020
Distribution: Nationwide

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Data last updated: November 6, 2026 ET

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.