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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: KS ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 27, 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 III

buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 60 count bottles, Rx Only, Manufactured for: Cipla USA Inc. 1560 Sawgrass Corporate Parkway Suite 130 Sunrise, FL 33323, Manufactured by: InvaGen Pharmaceuticals, Inc. (a subsidiary of Cipla Ltd.) Hauppauge, NY 11788 --- NDC 69097-877-03

by InvaGen Pharmaceuticals, Inc.

Reason: Failed Dissolution Specifications; during stability testing
Published: April 11, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC 51862-295-10.

by Mayne Pharma Inc

Reason: Superpotent Drug: High out of specification results for tazarotene assay at the 9-month stability time point.
Published: April 11, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Natural Grocers by Vitamin Cottage

Product: Natural Grocers Organic Coconut Smiles, 10 oz. plastic resea…
Reason: Coconut smiles product tested positive for Salmonella.
Published: April 11, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

The King Arthur Flour Company, Inc.

Product: King Arthur Flour, 100% Organic, Finely Ground, Coconut Flou…
Reason: Coconut flour tested positive for Salmonella.
Published: April 11, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

International Harvest, Inc.

Product: Coconut Smiles - Retail: International Harvest Brand Organic…
Reason: Product tested positive for Salmonella.
Published: April 11, 2018
Distribution: Directly distributed to the following st…

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FDA Recall Terminated Historical recordClass III

24-HOUR Oral Care q4 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health, Inc., 5405 Windward Parkway, Alpharetta, GA 30004; Distributed in the USA by Halyard Sales, LLC, Alpharetta, GA 30004, Product 97014.

by Akorn, Inc.

Reason: Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

24-HOUR Oral Care q2 Kit with Ballard* Technology, containing 2 Toothbrush Packs with CHG Solution, Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cup (NDC 50383-720-15), Rx Only, Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701; Kit Manufactured by Halyard Health, Inc., 5405 Windward Parkway, Alpharetta, GA 30004; Distributed in the USA by Halyard Sales, LLC, Alpharetta, GA 30004, Product 97012.

by Akorn, Inc.

Reason: Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Chlorhexidine Gluconate Oral Rinse, 0.12%, 15 mL unit dose cups (NDC 50383-720-15) packaged in 100-count (10 x 10) cups per case pack (NDC 50383-720-18 or 50383-720-19), Rx Only, Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701.

by Akorn, Inc.

Reason: Subpotent Drug: Product crystallization with accompanying low out of specification results for chlorhexidine assay.
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Fosphenytoin Sodium Injection, USP 500 mg PE*/10 mL, Made in India. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807, NDC 70121-1390-1

by Amneal Pharmaceuticals

Reason: Presence of particulate matter
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Evamist (estradiol transdermal spray), 1.53mg estradiol/spray, 0.27 fl oz (8.1 mL) per bottle, Rx Only, Manufactured for Perrigo, Minneapolis, MN 55427. NDC: 0574-2067-27

by Paddock Laboratories, LLC.

Reason: Defective Delivery System: Potential that cracks in the vial neck near the crimp may result in product evaporation and/or leaking and the inability to properly dispense product.
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Indomethacin Capsules USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403513, India; Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-302-01.

by Glenmark Pharmaceuticals Inc., USA

Reason: Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual adult dosage of "One or two capsules 2 or 3 times a day." rather than the correct usual adult dosage of "One capsule 2 or 3 times a day.
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Flucanazole Injection, USP 200 mg in in 100 mL (2 mg/mL), 10 Single Dose Flexible Containers, Rx Only, Manufactured for: Claris Lifesciences, Inc. North Brunswick, NJ 08902 By; Claris Injectables Ltd. Gujarat, India --- NDC 36000-006-10

by Renaissance Lakewood, LLC

Reason: Superpotent and Failed Stability Specifications; out of specification results for assay and water vapor permeability
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass I

Piggie Park Enterprises Inc

Product: Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bott…
Reason: Undeclared soy and wheat ingredients
Published: April 4, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Bourbon Brown Sugar Rub SE746665, 50# Bags
Reason: Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Published: April 4, 2018
Distribution: Domestic: PA, IL, AR, KS Foreign: Non…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Roast Grill Seasoning SE746664, 50# Bags
Reason: Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Published: April 4, 2018
Distribution: Domestic: PA, IL, AR, KS Foreign: Non…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Roast Chicken Marinade SE746125 and SE746126, 50# Bags
Reason: Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Published: April 4, 2018
Distribution: Domestic: PA, IL, AR, KS Foreign: Non…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Lbs, flv roast dark type, 30 # Boxes
Reason: Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Published: April 4, 2018
Distribution: Domestic: PA, IL, AR, KS Foreign: Non…

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FDA Recall United States Terminated Historical recordClass II

Newly Weds Foods Inc

Product: Au Jus Seasoning BM652767; bulk 50 lb boxes
Reason: Newly Weds Foods, Inc. initiated a voluntary recall of dry blended seasonings for industrial use due to a supplier's recall of yeast because of the presence of salmonella.
Published: April 4, 2018
Distribution: Domestic: PA, IL, AR, KS Foreign: Non…

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FDA Recall United States Terminated Historical recordClass I

Taylor Farms California Foodservice, Inc.

Product: Taylor Farms 3/8" Diced Yellow Onion 4/5# bags - 20 lb, corr…
Reason: Firm was notified by direct customer of a confirmed positive result for Salmonella ssp. after routine testing of the diced onion product.
Published: April 4, 2018
Distribution: OK, OH, MI, MN, IA, CA, KS, WI, PA, OR,…

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FDA Recall Terminated Historical recordClass III

Triamcinolone Acetonide Lotion, USP 0.1%, 60 mL bottle, Rx Only, Marketed by: VersaPharm Incorporated, Marietta, GA 30062; Manufactured by: Ei LLC, Kannapolis, NC 28083, NDC 61748-220-60.

by Akorn, Inc.

Reason: Failed Impurities/Degradation Specifications: High out of specification results for an impurity.
Published: March 28, 2018
Distribution: Nationwide

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Data last updated: September 27, 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.