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

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Source: FDA and USDA public dataLast updated September 25, 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

Sugar Foods Corporation Inc

Product: Fresh Gourmet Cubed Seasoned Croutons: 2.5 lb. foil pouch…
Reason: Recalled whey powder was used in further production of numerous food products.
Published: August 8, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Sugar Foods Corporation Inc

Product: Kitchen Fixins Zesty Italian Croutons: 5 oz. foil pouch It…
Reason: Recalled whey powder was used in further production of numerous food products.
Published: August 8, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Sugar Foods Corporation Inc

Product: Homestyle Seasoned Croutons: 4 oz. foil pouch Item # 73689…
Reason: Recalled whey powder was used in further production of numerous food products.
Published: August 8, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

General Mills, Inc

Product: Cheerios Protein Oats & Honey, Packaged in the following siz…
Reason: Cheerios Protein Oats and Honey cereal may be contaminated with Salmonella.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Pepsico Inc

Product: Diet Pepsi 7.5 oz cans, 6-pack. UPC on case label is 0 1200…
Reason: Diet Pepsi 7.5 oz cans, 6 pack, are recalled due to undeclared Aspartame.
Published: August 8, 2018
Distribution: distributed in AK, ID, MT, OR, and WA

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FDA Recall United States Terminated Historical recordClass III

Holmquist Hazelnut Orchards

Product: Ranch Flavored Hazelnuts in 4 oz Round Type, in plastic bag,…
Reason: Ranch Flavored Hazelnuts product is recalled due to undeclared hazelnut in the Contains statement.
Published: August 8, 2018
Distribution: distributed in WA and sold on company we…

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FDA Recall United States Terminated Historical recordClass II

Holmquist Hazelnut Orchards

Product: Butter Toffee Flavored Hazelnuts, packaged in a clear plasti…
Reason: Butter Toffee is recalled because milk is not declared on label. The Ingredient statement declares butter and the allergen Contains statement declares dairy.
Published: August 8, 2018
Distribution: distributed in WA and sold on company we…

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FDA Recall United States Terminated Historical recordClass I

LL'S MAGNETIC CLAY INC

Product: Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastro…
Reason: The recalled dietary supplement has the potential to contain undeclared allergens, including almonds, shellfish, milk, eggs, and peanuts.
Published: August 8, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30

by Aidarex Pharmaceuticals LLC

Reason: Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-90

by Aidarex Pharmaceuticals LLC

Reason: Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate, USP 2.5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0977-90

by Aidarex Pharmaceuticals LLC

Reason: Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10) Unit Dose per carton, Rx only, Manufactured by: Wockhardt Limited, H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054; Distributed by: MAJOR Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152; NDC 0904-5502-61.

by MAJOR PHARMACEUTICALS

Reason: Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate Tablets, USP, 2.5 mg, 100 Tablets (10 x 10) Unit Dose per carton, Rx only, Manufactured by: Wockhardt Limited, H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054; Distributed by: MAJOR Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152; NDC 0904-5609-61.

by MAJOR PHARMACEUTICALS

Reason: Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Testosterone Cypionate Injection, USP, 200 mg/mL, Rx only, 10 mL vials, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries, Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-016-40

by Sun Pharmaceutical Industries, Inc.

Reason: Presence of Particulate Matter: organic and inorganic compounds detected in vials of product.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Unit Dose Valsartan Tablets, USP. 160 mg. Rx only.,Distributed by: Major Pharmaceuticals, Livonia, MI 48152, NDC# 0904-6594-61. NDC# 0904-6595-61.

by MAJOR PHARMACEUTICALS

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Unit Dose Valsartan Tablets, USP, 80 mg. Rx only, Distributed by: Major Pharmaceuticals, Livonia, MI 48152, NDC# 0904-6594-61.

by MAJOR PHARMACEUTICALS

Reason: CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass III

Sisel International Llc

Product: Sisel, SiselRipt, postWORKOUT, Dietary supplement, net wt 5g…
Reason: Firm is recalling SiselRipt due to the presence of an unapproved artificial sweetener, Cyclamates.
Published: August 1, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PHENYLephrine 10 mg (PHENYLephrine HCL (USP) 10mg, 0.9% Sodium Chloride (USP) 250 mL. Volume: 251 mL Single dose bag. For: Redlands Community Hospital Pharmacy. BY: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 NDC 15082-856-25

by Avella of Deer Valley, Inc. Store 38

Reason: Lack of Assurance of Sterility: Potential leakage of bags.
Published: July 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, USP 50 mg in 0.9% Sodium Chloride, USP QS 10mL. 50 mg/10 mL (5 mg per mL). Volume 10 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-895-61

by Avella of Deer Valley, Inc. Store 38

Reason: Lack of Assurance of Sterility: Potential leakage of bags.
Published: July 25, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ePHEDrine Sulfate, USP 25 mg in 0.9% Sodium Chloride, USP QS 5mL. Volume 5 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-67

by Avella of Deer Valley, Inc. Store 38

Reason: Lack of Assurance of Sterility: Potential leakage of bags.
Published: July 25, 2018
Distribution: Nationwide

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Data last updated: September 25, 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.