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Recall totals

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

37,066

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 12, 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

IBU Ibuprofen Tablets, USP, 400 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a) NDC 55111-682-01 - 100 Tablets per bottle, b) NDC 55111-682-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 600 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-683-01 - 100 Tablets per bottle, b)NDC 5511-683-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.

by Dr. Reddy's Laboratories, Inc.

Reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b) 90-count bottle (NDC 68462-325-90), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Plot No. 2 Phase-2, Pharma Zone, SEZ, Pithampur, Dist-Dhar, Madya Pradesh - 454775, India Mfg Llc. No: 25/9/2010, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.

by Glenmark Pharmaceuticals Inc., USA

Reason: Failed Dissolution Specifications: below specification results
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

PARADISE DISTRIBUTORS, LLC

Product: Yummy brand Swirly Ices Assorted Flavors Net Wt. 2.3 ounces…
Reason: Undeclared milk.
Published: September 4, 2024
Distribution: Retail supermarkets in CA, NY, IL, FL, M…

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FDA Recall United States Terminated Historical recordClass I

PARADISE DISTRIBUTORS, LLC

Product: Yummy brand Swirly Ices Churning Cherry flavor Net Wt. 2.3 o…
Reason: Undeclared milk.
Published: September 4, 2024
Distribution: Retail supermarkets in CA, NY, IL, FL, M…

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FDA Recall United States Terminated Historical recordClass I

PARADISE DISTRIBUTORS, LLC

Product: Yummy brand Swirly Ices Fruity Melon flavor Net Wt. 2.3 ounc…
Reason: Undeclared milk.
Published: September 4, 2024
Distribution: Retail supermarkets in CA, NY, IL, FL, M…

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FDA Recall United States Terminated Historical recordClass I

PARADISE DISTRIBUTORS, LLC

Product: Yummy brand Swirly Ices Berry Blast flavor Net Wt. 2.3 ounce…
Reason: Undeclared milk.
Published: September 4, 2024
Distribution: Retail supermarkets in CA, NY, IL, FL, M…

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FDA Recall United States Terminated Historical recordClass I

PARADISE DISTRIBUTORS, LLC

Product: Yummy brand Swirly Ices Tropical Tornado flavor Net Wt. 2.3…
Reason: Undeclared milk.
Published: September 4, 2024
Distribution: Retail supermarkets in CA, NY, IL, FL, M…

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FDA Recall United States Terminated Historical recordClass II

NOW Foods

Product: NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag UP…
Reason: High mold, yeast, and total viable count
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Colonna Brothers Inc.

Product: Ground cinnamon. Supreme Tradition brand ground cinnamon p…
Reason: Elevated lead levels in cinnamon
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Prime Food Processing Corp.

Product: Prime Food brand Steam Bun with Egg Custard & Coconut Added;…
Reason: Products may contain undeclared sesame
Published: September 4, 2024
Distribution: AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY,…

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FDA Recall United States Terminated Historical recordClass I

Prime Food Processing Corp.

Product: Prime Food brand Steam Bun with Egg Custard Added; 10pcs/pac…
Reason: Products may contain undeclared sesame
Published: September 4, 2024
Distribution: AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY,…

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FDA Recall Ongoing Historical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, packaged in: a) 5mL bottle (NDC 64980-514-05), and b) 10mL bottle (NDC 64980-514-01), Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey

by FDC Limited

Reason: Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol), packaged in a) 3.78L (1-gallon jug packaged in a case of 4x1 gallon jugs), b) 18.92L (5-gallon pail), c) 208.19L (55-gallon drum), and d) 1040.98L (275-gallon tote), ZEE Company 3401 Cummings Road, Chattanooga, TN, 37419, NDC 86161-210

by Zeco LLC

Reason: CGMP Deviations: sterile water not used for production
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Rubbing Alcohol (70% Isopropyl Alcohol), First-Aid Antiseptic, packaged in a) 3.78L (1-gallon jug); and b) 208.19L (55-gallon drum), Sold by: ZEE Company- A Member of the Vincit Group, 3401 Cummings Road, Chattanooga, TN 37419, Made in USA.

by Zeco LLC

Reason: CGMP Deviations: sterile water not used for production
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

0.9% Sodium Chloride Injection USP, E8000, 1000mL container, Rx only, B. Braun Medical Inc., Irvine, CA, NDC 0264-7800-09.

by B. Braun Medical Inc

Reason: Presence of Particulate Matter
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales, PA 19454, NDC 0591-2925-30. Packet NDC # 0591-2925-32 Carton NDC # 0591-2925-30

by Teva Pharmaceuticals USA, Inc

Reason: Superpotent Drug
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lidocaine HCl Injection, 2% (20mg per mL) (100 mg per 5 mL) per syringe, Rx only, Fagron Sterile Services, 8710 E. 34th St, N. Wichita, KS 57226.

by Fagron Compounding Services

Reason: Lack of Assurance of Sterility
Published: August 28, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass I

Acetaminophen Injection, 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose bags, For Intravenous Use Only, Rx Only, Manufactured by: Hikma Farmaceutica (Portugal), SA, distributed by Hikma Pharmaceuticals USA Inc Berkeley Heights, NJ NDC 0143-9386-01

by Hikma Pharmaceuticals USA Inc.

Reason: Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL)
Published: August 28, 2024
Distribution: OH and PR

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Data last updated: September 12, 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.