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Recall totals

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

37,059

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/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 8, 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, 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 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

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 Terminated Historical recordClass II

Panaderia Salvadorena Ii

Product: PANADERIA/BAKERY Salvadorena; Quesadilla de Queso; Ingredien…
Reason: Product contains undeclared milk.
Published: April 23, 2025
Distribution: MA and RI

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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 III

Tristar Food Wholesale Co Inc

Product: BaiWei ShanZhuang, Dried Seedless Plum Candy, 9.16 oz. (260g…
Reason: Product contains cyclamates
Published: April 23, 2025
Distribution: The recalled product was distributed to…

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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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FDA Recall Ongoing Historical recordClass II

Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g), Distributed by Alchemee LLC, Santa Monica, CA 90401, Made in the USA, UPC 7 35786 01921 1, UPC 8 42944 10223 1, and also packaged as a twin pack UPC 8 42944 10241 5,

by Alchemee, LLC

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

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection, 100 mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Somerset, NJ 08873, NDC 70069-383-10

by Somerset Therapeutics Private Limited

Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection 100mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited, Kamataka, India, Manufactured for: BluePoint Laboratories NDC 68001-581-41 (individual carton) and NDC 68001-581-48 (5x1 mL cartons)

by Somerset Therapeutics Private Limited

Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured by: Somerset Therapeutics Limited, Kamataka India, Manufactured for: BluePoint Laboratories NDC 68001-580-41

by Somerset Therapeutics Private Limited

Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Haloperidol Decanoate Injection 50mg/mL, 1mL Single-Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Somerset, NJ 08873, NDC 70069-381-01 (individual carton) and NDC 70069-381-10 (10x1 mL carton)

by Somerset Therapeutics Private Limited

Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Methocarbamol Injection USP 1,000 mg/10 mL (100 mg/mL), 10 mL Single Dose Vial, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Somerset, NJ 08873, NDC 70069-101-25 (immediate carton) and 70069-101-05 (5x10 mL carton)

by Somerset Therapeutics Private Limited

Reason: Lack of Assurance of Sterility: Media fill with bacterial contamination
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 mL Plastic Irrigation Container (PIC), B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-2201-10

by B. Braun Medical Inc

Reason: Presence of Particulate Matter
Published: April 16, 2025
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Propafenone Hydrochloride Extended-Release Capsules, USP 325mg,60-count bottles, Rx Only, Mfd for: Northstar Rx LLC, Memphis, TN 38141, Mfd by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India. NDC# 16714-826-01

by Glenmark Pharmaceuticals Inc., USA

Reason: CGMP Deviations
Published: April 16, 2025
Distribution: Nationwide

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Data last updated: September 8, 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.