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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: PA ×
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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 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

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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 II

JJ Nuts, LLC

Product: MAGIC FLAME, HULLED SUNFLOWER KERNELS, BAKERY GRADE, 501b. B…
Reason: Glass fragments found in finished product.
Published: April 30, 2025
Distribution: The recalled product was distributed to…

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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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FDA Recall Ongoing Historical recordClass II

ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg, packaged in cartons of 100 TABLETS (10x10), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, NDC 0904-7129-61

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Reason: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg/100 mL (10 mg/mL), 1 x 100mL, Rx Only, Manufactured by: Gland Pharma Limited, Hyderabad, - 500 043 INDIA, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, NDC 43598-636-52

by Dr. Reddy's Laboratories, Inc.

Reason: LABELING: LABEL MIX-UP: The infusion bag is incorrectly labeled as Levetiracetam in 0.82% Sodium Chloride Injection 500 mg/100 mL, while the aluminum overwrap packaging correctly identifies the product as Levetiracetam in 0.75% Sodium Chloride Injection 1,000 mg/100 mL.
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Testosterone Cypionate Injection, USP, CIII, 200mg per mL, Rx only, 1mL Single-Dose Vial, Distributed by Eugia US LLC, E. Windsor, NJ, Manufactured by: Eugia Specialties Limited, Telangana State, India, NDC 55150-277-01

by Eugia US LLC

Reason: cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Unisom, SleepMinis, Diphenhydramine HCl, Mini-Capsules, 25 mg, 60 Mini-Capsules bottles, Dist. by Chattem, Inc., P.O. Box 2219, Chattanooga, TN 37409-0219, USA, UPC 0 41167 00670 2

by Chattem Inc

Reason: CGMP Deviations; detection of Nitrosamine Drug Substance-Related Impurities (NDSRI), N-nitroso-desmethyl-diphenhydramine (n-dph), above the FDA Recommended Intake Limit
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Blooming Import Inc.

Product: Golden Crop Candy (8 oz. (227g) un-wrapped candies)
Reason: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
Published: April 23, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

Blooming Import Inc.

Product: Golden Crop Candy (10 oz. (283g) wrapped candies)
Reason: Contains undeclared and unallowed colors (Blue 1, Red 40, Acid Red 18)
Published: April 23, 2025
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass II

TONY'S CHOCOLONELY INC

Product: Tony's Chocolonely Dark Chocolate Almond Sea Salt
Reason: Contains foreign objects (stones)
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

TONY'S CHOCOLONELY INC

Product: Tony's Chocolonely Everything Bar
Reason: Contains foreign objects (stones)
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Legally Addictive Foods

Product: LEGALLY ADDICTIVE THE O.G. COOKIES MADE FROM CRACKERS+TOFFEE…
Reason: The firm received complaints of a "rancid taste" from consumers.
Published: April 23, 2025
Distribution: IL & PA

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FDA Recall United States Terminated Historical recordClass I

Duda Farm Fresh Foods, Inc.

Product: Marketside brand celery stick. Net wt. 1.6 OZ. (45g); Rear p…
Reason: Product tested positive for Listeria Monocytogenes.
Published: April 23, 2025
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Reser's Fine Foods, Inc.

Product: Trader Joe's Hot Honey Mustard Dressing (SKU #80152), packag…
Reason: Undeclared peanuts, soy, sesame, and wheat.
Published: April 23, 2025
Distribution: Distributed in AR, CO, DC, DE, FL, GA, K…

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FDA Recall United States Terminated Historical recordClass III

Lins Waha International Corp

Product: Farmer House Preserve Olive Strips
Reason: Contains Cyclamates
Published: April 23, 2025
Distribution: Multiple states

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FDA Recall Ongoing Historical recordClass II

chlorproMAZINE Hydrochloride Tablets, USP 10 mg, Rx Only, 100 Tablets bottles, Manufactured by: Zydus Lifesciences Ltd., Baddi, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1129-1

by Zydus Pharmaceuticals (USA) Inc

Reason: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. oz. (177.4 mL), UPC 7 35786 01528 2; b) 0.33 OZ (9.45g), UPC 8 42944 10223 1; Distributed by Alchemee, LLC, Santa Monica, CA 90401,

by Alchemee, LLC

Reason: Chemical contamination: Presence of benzene
Published: April 16, 2025
Distribution: Nationwide

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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.