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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 26, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

Ceftriaxone for Injection USP, 250 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-611-01), and b) 10-count Vials per box (NDC 68180-611-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep 462 046 INDIA.

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: finished products manufactured using active pharmaceutical ingredients whose intermediates failed specifications.
Published: June 8, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Sulfacetamide Sodium Ophthalmic Solution, USP, 10%, Sterile, Rx Only, 15 mL bottles, Mfd. by: Akorn, Inc., Lake Forest, IL 60045 --- NDC 17478-221-12

by Akorn, Inc.

Reason: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness Testing on stability
Published: June 8, 2016
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

LGD-Xtreme (ligandrol LGD-4033),capsules, 3 mg, 90-count bottle, Manufactured for Continuum Labs, Fort Lauderdale, FL

by Invisiblu International LLC

Reason: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug, ligandrol LGD-4033
Published: June 8, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Licorice Coughing Liquid (guaifenesin), 5%, 3.38 fl. oz. (100 ml), OTC, Manufactured by: Ma Ying Long Pharmaceutical Group Co., LTD, Wuhan, China; Distributed by: Master Herbs (USA) Inc., NDC 68511-0460-01

by Master Herbs, Inc./Li

Reason: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Zhen Gong Fu, packaged in BIG BOX (16 small boxes / 2 capsules per box / 32 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Super Hard, packaged in BIG BOX (20 small boxes / 6 capsules per box / 120 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Samurai-X, packaged in BIG BOX (24 individually wrapped capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Tiger King, packaged in BIG BOX (10 small bottles / 10 capsules per bottle / 100 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Night Man, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Mojo Risen, packaged in BIG BOX (24 individual cards / 2 capsules per card/ 48 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Man King, packaged in BIG BOX (8 small boxes / 5 capsules per box / 40 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Hard Ten Days, packaged in BIG BOX (6 small boxes / 6 capsules per box / 36 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Plant Vigra, packaged in BIG BOX / (18 cans / 6 capsules per can / 108 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Happy Passengers, packaged in BIG BOX (30 small boxes / 1 capsule per box / 30 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Germany Niubian, packaged in BIG BOX (10 small boxes / 24 capsules per box / 240 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Black Storm, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Black Ant King, packaged in BIG BOX (10 capsules / can / 12 cans per box / 120 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Bigger Longer More Time More Sperms, packaged in BIG BOX (6 small boxes / 6 capsules per small box / 36 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

African Superman, packaged in BIG BOX (6 small boxes / 8 capsules per box / 48 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Zhong Hua Niu Bian, packaged in BIG BOX (6 small boxes / 6 capsules per box / 36 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467

by R Thomas Marketing, LLC

Reason: Marketed Without An Approved NDA/ANDA
Published: June 1, 2016
Distribution: Nationwide

View recall →

Data last updated: September 26, 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.