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Recall totals

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

37,139

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 24, 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 United States Terminated Historical recordClass II

Colorado Nut Co

Product: Honey Nutty Granola (8 oz. bag), UPC 018142352147. Packaged…
Reason: Undeclared milk in snack mix products
Published: December 20, 2017
Distribution: Product distributed distributors and ret…

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FDA Recall United States Terminated Historical recordClass II

Colorado Nut Co

Product: Oat Bran Nutty Crunch (8 oz. bag), UPC 018142352130. Package…
Reason: Undeclared milk in snack mix products
Published: December 20, 2017
Distribution: Product distributed distributors and ret…

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FDA Recall United States Terminated Historical recordClass II

Colorado Nut Co

Product: Cashew Cranberry Cherry Jubilee (8 oz. bag), UPC 01814235216…
Reason: Undeclared milk in snack mix products
Published: December 20, 2017
Distribution: Product distributed distributors and ret…

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FDA Recall Terminated Historical recordClass I

grande X 5800 capsule, (Maca Root 120 mg, Horny Goat Weed 120 mg, Guarana Seed 80 mg, Ginko Leaf 60 mg, Saw Palmetto 100 mg, Damiana Leaf 100 mg, Ginseng Root 80 mg, Tribulus Terrestris 90 mg, Tongkat Alo 100 mg, Rhodiola Rosea 60 mg, L-Arginine 90 mg), 1-capsule packets, distributed by Grande X Ontario, CA 91745, UPC 640793555440

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

FIFTY SHADES 6000 capsule, Proprietary Raw Material 4550, 1-capsule packets, distributed by Express Pac Trading, UPC 4026666146056

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

PapaZen 3300 capsule, Proprietary Blend 1800mg, 1-capsule packets, distributed by FX Power San Diego, CA 92108, UPC 718122032587

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

RHINO 7 Platinum 5000, capsule, Proprietary Material: 750mg, 1-capsule packets, distributed by Fifty Shades Bayside, NY 11361, UPC 617135861224

by Gadget Island, Inc

Reason: Marketed without an Approved NDA/ANDA: undeclared Active Pharmaceutical Ingredients sildenafil, desmethyl carbodenafil and tadalafil.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Pravastatin Sodium Tablets, USP, 40 mg, 30-count bottle, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-925-16

by International Laboratories, Inc.

Reason: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40 mg was filled with Bupropion hydrochloride XL Tablets 300 mg.
Published: December 13, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Paroxetine Tablets USP, 30 mg, a) 30 count (NDC 68382-099-06), b) 500 count (NDC 68382-099-05), and c) 1000 count (NDC 68382-099-10) count bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd, Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA, Inc., Pennington, NJ 08534

by Zydus Pharmaceuticals USA Inc

Reason: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Vertra Elemental Resistance (Octyl Methoxycinnamate 6%, Oxybenzone 5%, Titanium Dioxide 6.3%, Zinc Oxide 9.9%) Sun Protection Cream, SPF 50+, Net. Wt. 2.8 oz (80 g) tube in a carton, Distributed by Vertra/EAI-JR286, 20100 S Vermont Ave, Torrance, CA 90502, Made In Australia, UPC 8 94140 00103 0.

by EAI-JR286 INC

Reason: CGMP Deviations: products manufactured in a manner that may impact product quality that includes but is not limited to failed viscosity.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC 0574-0222-01

by Mayne Pharma Inc

Reason: Failed Dissolution Specifications.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Duloxetine Delayed-Release Capsules USP, 30 mg, 30-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Goa 403 722 India, NDC 68180-295-06, UPC 368180295068

by Lupin Pharmaceuticals Inc.

Reason: Failed Dissolution Specification
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Clozapine Tablets USP, 100 mg, 500 count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICALS IND, LTD, Jerusalem Israel, Manufactured For: TEVA PHARMACEUTICALS USA, North Wales, PA, NDC 00093-7772-05

by Teva Pharmaceuticals USA

Reason: Failed Tablet/Capsule Specifications; potential presence of broken tablets.
Published: December 6, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Dexamethasone Sodium Phosphate Injection, USP, 20 mg/5 mL (4 mg/mL), 5 mL Vials (NDC 0641-6146-01), packaged in 25 x 5 mL Vials per shelf pack (NDC 0641-6146-25), Rx Only, Manufactured by WEST-WARD, Eatontown, NJ 07724 USA.

by West-Ward Pharmaceuticals Corp.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Published: November 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Vials (NDC 0641-6145-01), packaged in 25 x 1 mL Vials per shelf pack (NDC 0641-6145-25), Rx Only, Manufactured by WEST-WARD, Eatontown, NJ 07724 USA.

by West-Ward Pharmaceuticals Corp.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
Published: November 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Columbus, Ohio 43217, NDC 68084-046-01

by Amerisource Health Services

Reason: Presence of Foreign Tablets/Capsules.
Published: November 29, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Lorazepam Tablets, USP CIV, 0.5 mg, 500-count bottle, Rx Only, Manufactured by: Leading Pharma, LLC Fairfield, NJ 07004 NDC 69315-904-05

by Leading Pharma, LLC

Reason: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam
Published: November 29, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Shoreline Fruit, LLC

Product: Shoreline Fruit Dark Choc Covered Montmorency Cherries packa…
Reason: Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.
Published: November 29, 2017
Distribution: Domestic: AK AL AR AZ CA CO CT DC…

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FDA Recall United States Terminated Historical recordClass II

Shoreline Fruit, LLC

Product: Dried Dark Chocolate Covered Cherries, The products are pack…
Reason: Shoreline Fruit is voluntarily recalling select Shoreline Fruit bulk and Cherry Bay Orchards branded dark chocolate coated cherry products due to supplier's recall of undeclared allergen milk in dark chocolate.
Published: November 29, 2017
Distribution: Domestic: AK AL AR AZ CA CO CT DC…

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FDA Recall Terminated Historical recordClass III

Meclizine hydrochloride tablets USP, 12.5 mg, 100 count HDPE bottle, Rx only, Manufactured by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-122-06

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Published: November 22, 2017
Distribution: Nationwide

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Data last updated: September 24, 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.