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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

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

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Source: FDA and USDA public dataLast updated September 10, 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 United States Terminated Historical recordClass I

Sysco Corporation

Product: 3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT…
Reason: Cucumbers have the potential to be contaminated with Salmonella
Published: June 18, 2025
Distribution: DC, DE, FL, GA, MA, MD, MI, NC, NJ, OH,…

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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

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FDA Recall United States Terminated Historical recordClass III

R&M TRADING LLC

Product: Instant Milk Tea Matcha Flavor, R&M Refresher brand, B0D71Y8…
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 Taro Flavor, R&M Refresher brand, B0D72CMLB…
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 Honeydew Flavor, R&M Refresher brand, B0D72…
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 Ongoing Historical recordClass II

Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5

by Consumer Product Partners, LLC

Reason: Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
Published: June 11, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4

by Apotex Corp.

Reason: Defective Container: This recall is being initiated due to a leaking unit stored horizontally.
Published: June 11, 2025
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-91 (Carton); 13668-473-70 (Blister)

by Torrent Pharma Inc.

Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published: June 11, 2025
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Fluoxetine Tablets, USP, 20 mg, 30-count bottle, Rx only, Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-30

by Torrent Pharma Inc.

Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.
Published: June 11, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, 30 capsules (3 x 10 blister cards) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-411-21 (carton), NDC 68084-411-11 (blister card).

by Amerisource Health Services LLC

Reason: cGMP deviations
Published: June 11, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

VAUGHAN MILLS PACKAGING LTD.

Product: Giant, Instant Oatmeal Raisins and Spice, 10 -1.5 oz. Packet…
Reason: Undeclared Allergen (walnuts), was not on outer packaging but was on the inner packaging of product.
Published: June 11, 2025
Distribution: The recalled product was distributed to…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product: AMCE GREEK SALAD AUTHENTIC FS, Refrigerated, packaged in cle…
Reason: Salmonella. Greek Salad products were made with recalled cucumbers from Bedner Grower's Company which are contaminated with Salmonella and implicated in an ongoing outbreak.
Published: June 11, 2025
Distribution: Distributed in Connecticut, Delaware, Ma…

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FDA Recall United States Terminated Historical recordClass III

GNC Holdings LLC

Product: GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet…
Reason: Undeclared Fish allergen (parvalbumin).
Published: June 11, 2025
Distribution: The adulterated product was distributed…

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FDA Recall Ongoing Historical recordClass I

ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N

by EnShiShiXiangNiShangMaoYouXianGongSi

Reason: Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
Published: June 4, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colvale-Bardez, Goa - 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-356-01

by Glenmark Pharmaceuticals Inc., USA

Reason: OOS results reported for the Dissolution (by UV) test.
Published: June 4, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-165-05.

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-164-05

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
Published: June 4, 2025
Distribution: Nationwide

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Data last updated: September 10, 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.