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Recall totals

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

37,063

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/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 11, 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 Terminated Historical recordClass II

clomiPRAMINE hydrochloride Capsules USP, 25 mg, 100-count bottle, Rx only, Manufactured For: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, United States, Manufactured By: Lupin Limited, Nagpur, 441 108 INDIA, NDC 68180-492-01

by Lupin Pharmaceuticals Inc.

Reason: Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability study.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Ketamine HCl 50mg per 5mL (10 mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112.NDC: 71449-068-11

by Denver Solutions, LLC DBA Leiters Health

Reason: Lack of Assurance of Sterility: Leaking/damaged syringes.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,

by Denver Solutions, LLC DBA Leiters Health

Reason: Lack of Assurance of Sterility: Leaking/damaged syringes.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.

by Denver Solutions, LLC DBA Leiters Health

Reason: Lack of Assurance of Sterility: Leaking/damaged syringes.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Glycopyrrolate, 1mg per 5mL, (0.2 mg/mL), Single Dose 5 mL syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC 71449-104-11

by Denver Solutions, LLC DBA Leiters Health

Reason: Lack of Assurance of Sterility: Leaking/damaged syringes.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 30 mg, a.) 90-count bottles (NDC# 51991-747-90), b.) 1000-count bottles (NDC 51991-747-10), Rx Only, Manufactured by Towa Pharmaceutical Europe, S.L. Distributed by Breckenridge Pharmaceutical, Inc. Berkeley Heights, NJ 07922

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Duloxetine Delayed-Release Capsules USP, 60 mg, 1000-count bottles, Rx Only, Manufactured by Towa Pharmaceutical Europe, S.L., Distributed by Breckenridge Pharmaceutical, Inc. Berkeley Heights, NJ 07922, NDC# 51991-748-10

by Breckenridge Pharmaceutical, Inc

Reason: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Bimatoprost powder, Bulk Ingredient, a) 5g (NDC 38779-3066-03), b) 1g (NDC 38779-3066-06), c) 1g (NDC 38779-3066-09) drums, Medisca, Plattsburgh, NY

by Medisca Inc.

Reason: CGMP Deviations
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Rocuronium Bromide 50 mg per 5mL (10mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-004-11

by Denver Solutions, LLC DBA Leiters Health

Reason: Lack of Assurance of Sterility: Leaking/damaged syringes.
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection, 100mg/mL*, 5 x 1 mL Single-Dose Vials, Rx Only, Manufactured by: Somerset Therapeutics Limited, #54/1 Boodhihal Village, Nelamangala, Bangalore -562123, Karnataka, India, Manufactured for: BluePoint Laboratories, NDC 68001-581-48.

by Amerisource Health Services LLC

Reason: Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection, 100 mg/mL*, 1 x 1 mL Single-Dose Vial, Rx only, Manufactured by: Somerset Therapeutics Limited, #54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka, India, Manufactured for BluePoint Laboratories, NDC 68001-581-41.

by Amerisource Health Services LLC

Reason: Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Published: April 30, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection, 50mg/mL* , 1 mL Single-Dose Vial, Rx only, Manufactured by Somerset Therapeutics Limited, 54/1, Boodhihal Village, Nelamangala, Bangalore - 562123, Karnataka, India, Manufactured for: BluePoint Laboratories, NDC 68001-580-41.

by Amerisource Health Services LLC

Reason: Lack of assurance of sterility. Bacterial contamination detected in some media fill units
Published: April 30, 2025
Distribution: Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

Supherb Farms

Product: Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT:…
Reason: Potential contamination with foreign objects.
Published: April 30, 2025
Distribution: United States: CA, MA, MI, NY, OH, OR, T…

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FDA Recall United States Completed Historical recordClass II

Supherb Farms

Product: Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FRO…
Reason: Potential contamination with foreign objects.
Published: April 30, 2025
Distribution: United States: CA, MA, MI, NY, OH, OR, T…

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Beecher's Street Corn, 18oz, 8 retail units per case, UPC 78…
Reason: Potential contamination with foreign material (wood)
Published: April 30, 2025
Distribution: IL and MI

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Cuban-Style Black Bean Soup, 4 / 4lb pouches, Net Wt. 16lb
Reason: Potential contamination with foreign material (wood)
Published: April 30, 2025
Distribution: IL and MI

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Mexican Street Corn Soup, 4 / 4lb pouches, Net Wt. 16lb
Reason: Potential contamination with foreign material (wood)
Published: April 30, 2025
Distribution: IL and MI

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FDA Recall United States Terminated Historical recordClass II

Request Foods Incorporated

Product: Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb
Reason: Potential contamination with foreign material (wood)
Published: April 30, 2025
Distribution: IL and MI

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FDA Recall United States Terminated Historical recordClass II

S Martinelli & Company

Product: Apple Juice; clear/translucent bulbous/round glass bottle wi…
Reason: Potential contamination with patulin.
Published: April 30, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

Walker's Fruit Basket and Press House

Product: Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60, 275 gallo…
Reason: May be contaminated with Clostridium botulinum
Published: April 30, 2025
Distribution: Multiple states

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Data last updated: September 11, 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.