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Recall totals

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

37,060

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 9, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall Ongoing Historical recordClass II

DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL (34 fl. oz.) per bag (NDC 61924-092-34), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

DermaCerin, Skin Protectant Moisturizing Cream (petrolatum 33%), packaged in a) 106 g (3.75 oz.) per tube (NDC 61924-174-04) and b) 454 g (16 oz.) per jar (NDC 61924-174-16), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04

by DermaRite Industries, LLC

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Bromocriptine Mesylate Capsules, USP, 5 mg, 30 Capsules per bottle, Rx Only. Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals, Pennington, NJ 08534. NDC 68382-110-06

by Zydus Pharmaceuticals (USA) Inc

Reason: Failed Impurities/Degradation Specifications: Out of Specification (OOS) result reported for 2- Bromoergine impurity of Bromocriptine Mesylate Capsules.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90

by Golden State Medical Supply Inc.

Reason: Failed Dissolution Specifications
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Klarity-C Drops (Cyclosporine) 0.1%, Preservative-Free Sterile Ophthalmic Emulsion, This is a compounded drug, Office Use Only, 5.5 mL bottle, Rx only, Mfg by: Imprimis NJOF, LLC, 1705 Route 46 West, Ledgewood, NJ 07852, NDC 71384-514-05

by Imprimis NJOF, LLC

Reason: Subpotent Drug
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Fesoterodine Fumarate, Extended-release Tablets, 4 mg, 30-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited, Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-175-30

by Alembic Pharmaceuticals Limited

Reason: Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Published: November 26, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Peterson Company Inc

Product: Item# 29608 Farmhouse White, Twin Sisters Creamery brand, pr…
Reason: Item #29608 Farmhouse White is recalled due to E. coli O103:H2.
Published: November 26, 2025
Distribution: Press release indicates products were di…

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FDA Recall United States Terminated Historical recordClass I

Peterson Company Inc

Product: Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, produ…
Reason: Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
Published: November 26, 2025
Distribution: Press release indicates products were di…

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FDA Recall United States Terminated Historical recordClass I

Twin Sisters Creamery, LLC

Product: Twin Sisters Creamery Mustard Seed cheese, 3lb. round cheese…
Reason: Raw milk Mustard Seed cheese is recalled due to E. coli O103:H2 and E. coli O74:H25.
Published: November 26, 2025
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass I

Twin Sisters Creamery, LLC

Product: Twin Sisters Creamery Peppercorn cheese, 3lb. round cheese w…
Reason: Raw milk Peppercorn cheese is recalled due to E.coli O26:H11
Published: November 26, 2025
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass I

Twin Sisters Creamery, LLC

Product: Twin Sisters Creamery Farmhouse Cheese, 3lb. round cheese wh…
Reason: Raw milk Farmhouse cheeses are recalled due to E. coli O103:H2 and E. coli O74:H25.
Published: November 26, 2025
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass I

Twin Sisters Creamery, LLC

Product: Twin Sisters Creamery Whatcom Blue cheese, 2.5lb. round chee…
Reason: Raw milk Whatcom Blue cheese is recalled due to E. coli O103:H2.
Published: November 26, 2025
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

HANA GROUP

Product: Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Pla…
Reason: Wheat and Soy missing allergens from the product Contains Statement.
Published: November 19, 2025
Distribution: (FL, VA, IL, NE, MN, IN, LA, OK) - retai…

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FDA Recall United States Terminated Historical recordClass I

JFE FRANCHISING INC

Product: Peach Salsa - $5.99-16 oz 639123940636 packaged in clear pla…
Reason: Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Published: November 19, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

GBC Food Services, LLC

Product: Peach Salsa; UPC 85006540364 14oz (397g); Use by 10/12/2025…
Reason: Peaches provided by Moonlight Peaches potentially contaminated with Listeria.
Published: November 19, 2025
Distribution: IL, CO, GA, WA, IN, MS, TN, AR, OR, MI.

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FDA Recall United States Terminated Historical recordClass I

Seoul Trading, Inc.

Product: Item IL1014A, PIGGY Lotte Crispy Crunch Ice Cream Cone, Stra…
Reason: Undeclared peanut.
Published: November 19, 2025
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass I

Lotus Vaping Technologies, LLC

Product: Monarch Premium Kratom White Elephant powder is packaged in…
Reason: Product has the potential to be contaminated with Salmonella
Published: November 19, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lotus Vaping Technologies, LLC

Product: Monarch Premium Kratom Red Bali powder is packaged in seal m…
Reason: Product has the potential to be contaminated with Salmonella
Published: November 19, 2025
Distribution: Nationwide

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Data last updated: September 9, 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.