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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: NV ×
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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

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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 II

Ibuprofen Tablets, USP, 200 mg, a) 50 tablets (NDC 49483-601-05), b) 100 tablets (NDC- 49483-601-01), c) 500 tablets (NDC 49483-601-50), d) 1000 tablets (NDC 49489-601-10), e) Bulk (49483-601-00) bottles, Brown, Manufactured for: Time Cap Labs, Inc., Farmingdale, NY 11735, Manufactured by: Marksans Pharma, Ltd., Verna, Goa-403 722, India

by Time-Cap Laboratories, Inc.

Reason: CGMP Deviations: Various strengths of ibuprofen tablets/caplets are being recalled due to complaints of odor related to CGMP deficiencies.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

NGB, Corp

Product: Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 c…
Reason: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella contamination.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small…
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: MMRF Neyyappam, UPC: 870400000111, Frozen
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: MMRF Kumbiliappam, UPC: 87040000104, Frozen
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Maharaja Food Importers, Inc.

Product: ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
Reason: Label states ghee, but does not declare milk.
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product: Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoo…
Reason: Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Seabear Company

Product: Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Ox…
Reason: Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
Published: May 2, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 40 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Estradiol 25 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Estradiol 20 mg (SD) pellets in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800.

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Testosterone 25 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Testosterone 100 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Testosterone 200 mg pellet packaged in amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

MVI-7 (B1-100mg/B3-100mg, B5-252 mg, B6-102mg, Vit C-2500 mg, B12-10mg, Mag-1000 mg)/ vial liquid injectable, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Naltrexone 200 mg pellet, amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Methionine 25mg/Inositol 50mg/Choline 50mg/ B12 1mg, 50 mL amber vial, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. #101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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FDA Recall Terminated Historical recordClass II

Vitamin D 50,000 unit/ml, 5 mL amber vial, Injectable Liquid, Rx only, Partell Specialty Pharmacy, 5835 S. Eastern Ave. # 101, Las Vegas, NV 89119 (702) 791-3800

by Partell Specialty Pharmacy

Reason: Lack of Assurance Sterility: Firm is recalling various drug products due to a non-approved method of sterilization.
Published: April 25, 2018
Distribution: NV only

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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.