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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Reese Pharmaceutical Company

Product: Berry Flavor Immune Support Dietary Supplement Effervescent…
Reason: The label does not list "Sodium" in the ingredient statement.
Published: December 6, 2017
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Pacific Rim Distribution Inc.

Product: Bean Boy Coffee Dark Chocolate Covered Espresso Beans
Reason: Pacific Rim Distribution Inc., dba Bean Boy Coffee is voluntarily recalling Dark Chocolate Covered Espresso Beans following a supplier's recall due to undeclared allergen milk.
Published: December 6, 2017
Distribution: Domestic: MI, OH, GA, AZ Foreign: Can…

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FDA Recall United States Terminated Historical recordClass II

Dutch Valley Food Distributors Inc.

Product: Dark Chocolate Cashew, Net 11 oz., Contains Cashew and Soy,…
Reason: Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
Published: December 6, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Dutch Valley Food Distributors Inc.

Product: Dark Chocolate Almond, Net 11 oz., Contains Almond and Soy,…
Reason: Our supplier, GKI, did not have milk declared as an allergen on an item we repackage. Therefore our labels did not contain milk
Published: December 6, 2017
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Gourmet Nut, Inc.

Product: GourmetNut DARK CHOCOLATE COVERED ALMONDS NET WT 7oz (198g);…
Reason: Product contains undeclared milk.
Published: December 6, 2017
Distribution: Multiple states

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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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FDA Recall Terminated Historical recordClass II

Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3) and d) 100 G bottle (NDC 51552-1392-5), Rx only, Distributed by Fagron, Inc., 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel. 1-(800) 423-6967

by Fagron, Inc

Reason: cGMP Deviations: lack of quality assurance at the API manufacturer.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lumigan (bimatoprost ophthalmic solution) 0.01%, 2.5 mL bottle, Rx only, Allergan, Irvine, CA 92612. NDC# 0023-3205-03

by Allergan Sales, LLC

Reason: Failed Impurities/Degradation Specifications.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Combigan (brimonidine tartrate/timolol maleate ophthalmic solution) 0.2%/0.5%, Rx only, packaged in a) 2.5 mL NDC# 0023-9211-03; b) 5 mL (NDC# 0023-9211-05); c) 10 mL (NDC# 0023-9211-10); d) 15 mL (NDC# 0023-9211-15) bottles, Manufactured By: Allergan, Irvine, CA 92612..

by Allergan Sales, LLC

Reason: Failed Impurities/Degradation Specifications.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clolar (clofarabine) 20 mg/20 mL (1 mg/mL) Injection, for intravenous use, Rx Only, Mfd. by: Teva Pharmachemie Swensweg 5 Haarlem, The Netherlands Mfd. for: Genzyme Corporation, Cambridge, MA 02142, NDC 0024-5860-01.

by Genzyme Corporation

Reason: Labeling: Incorrect or Missing Package Insert.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only. Packaged and Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC: 68084-390-01

by Amerisource Health Services

Reason: Failed Stability Specifications
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

doTERRA International, LLC

Product: Slim & Sassy¿ TrimShake Chocolate, SKU 35200001, 1 lb 5.9…
Reason: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake - Chocolate and Slim & Sassy¿ TrimShake Vanilla mixes due to an undeclared milk allergen.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

doTERRA International, LLC

Product: Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz,…
Reason: doTERRA is voluntarily recalling unexpired Slim & Sassy¿ TrimShake - Chocolate and Slim & Sassy¿ TrimShake Vanilla mixes due to an undeclared milk allergen.
Published: November 22, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Aurora Products, Inc.

Product: Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in :…
Reason: Product contains undeclared milk
Published: November 22, 2017
Distribution: Nationwide

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Data last updated: September 30, 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.