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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 12, 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 Terminated Historical recordClass III

Xolegel (ketoconazole) gel 2%, 45 gram tubes, Rx only, Manufactured by: DPT Laboratories, San Antonio, TX 78215, NDC 16110-080-45

by ALMIRALL, LLC

Reason: Failed Viscosity specification: Slightly higher OOS results obtained for viscosity
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Rifampin Capsules, USP, 300 mg, a) 30-count bottle (NDC 61748-018-30), b) 60-count bottle (NDC 61748-018-60), c) 100-count bottle (NDC 61748-018-01), Rx only, Distributed by: Akorn Operating Company, LLC, Gurnee, IL 60031.

by Akorn, Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Distributed by: Akorn Operating Company, LLC, Gurnee, IL 60031, NDC 61748-015-30

by Akorn, Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

ClomiPRAMINE Hydrochloride Capsules, USP 25mg, 100-count bottles, Rx only, LEADING PHARMA, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-167-01

by Leading Pharma, LLC

Reason: Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Budesonide Inhalation Suspension 0.25mg/2mL, For Inhalation Only, Rx Only, 1 envelope x five 2 mL Single Dose Ampules per pouch, Sterile Suspension, Manufactured by: Cipla Ltd., India, Manufactured for Cipla USA Inc., Warren NJ, NDC# 69097-318-86.

by CIPLA

Reason: Lack of Assurance of Sterility
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride, Injection for IV Use, High Alert, This is a Compounded Product for Institutional or Office Use Only, Not for Resale, QuVa PHARMA 519 Route 173, Bloomsbury, NJ 08804, Total volume: 500 mL bag, NDC: 70092-1068-07.

by QuVa Pharma, Inc.

Reason: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Neoral soft gelatin capsules (cyclosporine capsules, USP) Modified, 25 mg, Rx Only, 30 Soft Gelatin Capsules per carton, Mfg by: Novartis Pharmaceuticals Corporation, East Hanover, NJ 07936, NDC # 0078-0246-15.

by Novartis Pharmaceuticals Corporation

Reason: CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10, Rx only, Mylan Manufactured in India for: Mylan Institutional LLC Rockford, IL 61103 U.S.A

by Viatris Inc

Reason: Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Esomeprazole Magnesium Delayed-Release Capsules, USP, 40mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories Inc. New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 63304-735-90.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Rx Only, 90 Capsules per bottle, Manufactured by: Ohm Laboratories Inc. New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 63304-734-90.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

World Variety Produce Inc dba Melissa's

Product: Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1…
Reason: Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did not declare the allergen of egg.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lamb Weston Sales

Product: Item SP204, Sprouts Organic Hash Browns Shredded Potatoes, 1…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lamb Weston Sales

Product: Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Lamb Weston Sales

Product: Item AX058, Alexia Organic Seasoned Hashed Browns Yukon Sele…
Reason: Potential to be contaminated with Listeria monocytogenes.
Published: October 5, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100-count bottle, Rx Only, Manufactured by: UNICHEM LABORATORIES LTD. Pilerne Ind. Estate, Pilerne, Bardez, Goa 403 511, India Manufactured for: UNICHEM PHARMACEUTICALS (USA), INC. East Brunswick, NJ 08816. NDC# 29300-137-01

by UNICHEM PHARMACEUTICALS USA INC

Reason: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets,
Published: September 28, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Pepsico Inc

Product: Mountain Dew Major Melon Zero, 12 FL OZ (355mL) can, sold as…
Reason: The outer wraps match the liquid in the can (Zero Sugar - Mountain Dew Major Melon) however the primary package (can) is incorrect (Full Sugar Mountain Dew Major Melon). Product inside can matches the product/nutritional panel on the point-of-sale outer container wrap.
Published: September 28, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL), packaged in 100 mL glass fliptop vial (NDC 0409-4699-54) further packaged in a tray of 10 vials (NDC Carton: 0409-4699-24), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA

by Pfizer Inc.

Reason: Presence of particulate matter
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, Rx Only, 100 tablets per bottle, Teva Pharmaceuticals USA, Inc. North Wales, PA 19454, NDC 0555-0777-02.

by Teva Pharmaceuticals USA Inc

Reason: Labeling: Label Error on Declared Strength; A sealed 100-count bottle labeled with 15 mg actually contained 100 tablets of 20 mg strength of the drug product.
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Synergy Hand Sanitizer, Non-Sterile Solution to help reduce bacteria that can potentially cause disease, For use when soap and water are not available, Alcohol 80% Topical Solution, Antiseptic, 8.5 oz./ 250 mL bottles, Made and Distributed by: Superior Glove Works Ltd., 36 Vimy Street, Acton, Ontario, L7J 1S1, Canada, Made in Canada, UPC: 779406201594.

by SUPERIOR GLOVE WORKS, LTD.

Reason: CGMP Deviations: FDA analysis found product to contain acetaldehyde impurity and the Sum of All Impurities, above specification limits.
Published: September 21, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lisinopril Tablets USP, 10 mg, 1000-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Nagpur- 441 108, India. NDC 68180-980-03

by Lupin Pharmaceuticals Inc.

Reason: Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Published: September 21, 2022
Distribution: Nationwide

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Data last updated: September 12, 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.