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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: RI ×
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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 United States Terminated Historical recordClass II

Youngstown Grape Distributors, Inc.

Product: Happy Moose Juice Tropical Roots packaged in a plastic 12 fl…
Reason: Incomplete pasteurization
Published: October 30, 2024
Distribution: CA, TX, WA, KY, NC, NY, IL, VA, AL, GA,…

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FDA Recall Ongoing Historical recordClass II

First Aid Antiseptic Ointment, Povidone Iodine USP 10%, Inactive Ingredients: mineral oil, petrolatum. NET Wt. 1 OZ (28.4 g) per tube, Distributed by: Rugby Laboratories, Indianapolis, IN 46268. Made in China. NDC: 0536-1271-80

by Zhejiang Jingwei Pharmaceutical Co., Ltd.

Reason: Incorrect/Undeclared Excipients: The inactive ingredients labeled on the product boxes and tubes are listed as "mineral oil , petrolatum ". The inactive ingredients in the actual product are polyethylene glycol 400 , polyethylene glycol 4000.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Atovaquone Oral Suspension, USP 750 mg/5 mL, 210 mL bottle, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, NDC # 69452-252-87.

by Bionpharma Inc.

Reason: Microbial Contamination of a Non-sterile Product: The product was found to be contaminated with Cohnella bacteria.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Cisplatin Injection, 100mg/100mL (1mg/mL), For Intravenous Use, 100 mL Multiple Dose Vial, Rx Only, Manufactured for: Accord Healthcare Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad 382 213, India. Mfg. Lic. No.: G/28/1336, NDC 16729-288-38

by ACCORD HEALTHCARE, INC.

Reason: Failed Impurities/Degradation Specifications.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Duloxetine Delayed-Release Capsules, USP, 20mg, Rx Only, 500-count bottles, Mfr. by: Towa Pharmaceutical Europe, S.L. Distributed by: BPI, NDC 51991-746-05.

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Gorilla Mind LLC

Product: Gorilla Mind Rauwolscine Dietary Supplement, Suppress Appeti…
Reason: Product was recalled due to the potential for contamination with Salmonella
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nuts.com

Product: S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranf…
Reason: Undeclared Allergen, milk - a mix-up between the product description and the ingredient list. Milk Chocolate was listed in the product description but was missing from the ingredient list.
Published: October 23, 2024
Distribution: The adulterated product was distributed…

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FDA Recall United States Terminated Historical recordClass II

Hydration Labs Inc. dba Bevi

Product: Flavor#115 Electrolytes, Net Contents 3.78L, #740-0115, GTIN…
Reason: Product is labeled as electrolytes but is actually caffeine
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Walmart Inc

Product: Great Value Cherry Mixed Fruit, 4 oz, 4 Count and 12 count p…
Reason: FD&C Red No 3 was not declared as an ingredient.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Walmart Inc

Product: Great Value Diced Peaches, Mandarin Segments, & Cherry Mixed…
Reason: FD&C Red No 3 was not declared as an ingredient.
Published: October 23, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Ryaltris (olopatadine hydrochloride and mometasone fluorate) Nasal Spray, 665 mcg/25 mcg per spray, 240 Metered Sprays/bottle, 29 g net fill weight, Distr. by Hikma Specialty USA Inc., Columbus, OH 43328, hikma, Glenmark Specialty SA. NDC 59467-700-27.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Delivery System: The dip tube is clogged causing the spray not to work.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2

by Gilead Sciences, Inc.

Reason: Presence of Particulate Matter: Presence of glass particle.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199

by Supercore Products Group Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Hard Steel Capsules packaged in 1 count blister packs in boxes of 10, 20 and 30, Manufactured in U.S.A.

by Supercore Products Group Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass III

Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c) 100 gm Tube, NDC 68462-0455-94, Manufactured by: Glenmark Pharmaceuticals, Ltd., Colvale-Bardez, Goa 403513, India, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Defective Container: Firm received complaints of broken tube at the seal.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Atorvastatin Calcium Tablets, USP, 40mg, Rx only, 1000 Tablets per bottle, Manufactured for: Nivagen Pharmaceuticals, Inc. Sacramento, CA 95827, USA, Manufactured by: Umedica Laboratories Pvt Ltd., Vapi Gujarat 396195, India, NDC: 75834-257-01.

by Nivagen Pharmaceuticals Inc

Reason: Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Blue Tape Sriracha

Product: Blue Tape Sriracha sauce is refrigerated condiment, packaged…
Reason: Acidified product was manufactured by firm without ODA license.
Published: October 9, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Mycophenolic Acid Delayed-Release Tablets USP, 360 mg, Rx Only, 120 Tablets per bottle, Manufactured by Alkem Laboratories, LTD, INDIA; Distributed by Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-427-12.

by Ascend Laboratories, LLC

Reason: Failed Dissolution Specifications
Published: October 2, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules, Distributed by: Guru Inc., 4370 Lawrenceville Hwy NW, P.O. Box 2204, Lilburn, GA 30047-1100, USA. Ph.: 872 216 1566, http://www.dalayurevda.com, Made in India, UPC: 042535355019

by Guru Inc.

Reason: Marketed without an approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac, and phenylbutazone.
Published: October 2, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Refresh LACRI-LUBE, (42.5% Mineral Oil, 57.3% White Petrolatum) Lubricant Eye Ointment, Net wt, 0.12 oz (3.5g) Tube, Distributed by: Allergen, an AbbVie company, Madison, NJ 07940, UPC code: 300230312042

by AbbVie Inc.

Reason: Lack of Assurance of Sterility: The impacted lots may contain a breach in the tube seal.
Published: October 2, 2024
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.