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Recall totals

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

37,271

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,852

Class I recallsReasonable probability of serious health consequences

24,397

Class II recallsTemporary or medically reversible health consequences

2,897

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 2,085 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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 October 19, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,397
Class I	9,852
Class III	2,897
Not Yet Classified	2

FDA Recall TerminatedTerminated: April 29, 2025Historical recordClass II

Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01

by Lupin Pharmaceuticals Inc.

Reason: Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
Published: September 4, 2024
Distribution: Nationwide

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FDA Recall OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 TerminatedTerminated: December 16, 2025Historical 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 TerminatedTerminated: November 7, 2024Historical 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 TerminatedTerminated: August 4, 2025Historical recordClass II

PBM Nutritionals, LLC

Product: CVS Health brand and HEB Baby brand Premium Infant Formula w…
Reason: Product contains levels of Vitamin D above the maximum level permitted.
Published: September 4, 2024
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: April 11, 2025Historical 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 TerminatedTerminated: April 11, 2025Historical 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 OngoingHistorical 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 OngoingHistorical recordClass I

Healthy Living Acetaminophen, Aspirin (NSAID) and Caffeine, tablets USP, 250 mg/250 mg/65 mg, 100-count bottles, Distributed by: Aurohealth LLC, 279 Princeton-Hightstown Road, East Windsor, NJ , Made in India, NDC 58602-882-21.

by Aurobindo Pharma USA Inc

Reason: Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Published: August 28, 2024
Distribution: NJ, NY & PA

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FDA Recall CompletedHistorical 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 CompletedHistorical 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 OngoingHistorical 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 OngoingHistorical 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 OngoingHistorical 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 United States TerminatedTerminated: March 14, 2025Historical recordClass II

Refresco Beverages US Inc

Product: Great Value; 8oz Apple Juice in 6 pack; 100% Juice; packaged…
Reason: Product contains inorganic arsenic above action level set in industry guidance (13.2ppb)
Published: August 28, 2024
Distribution: Retail locations in: AL, CT, DC, DE, FL,…

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FDA Recall OngoingHistorical recordClass II

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, [NDC 64980-514-05].

by FDC Limited

Reason: Defective container; yellow colored spike from cap lodged in the nozzle
Published: August 21, 2024
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 27, 2024Historical recordClass I

RS Hanline and Company Inc

Product: Green Peppers packaged as whole 10lb carton, whole 20lb cart…
Reason: Potential contamination with Listeria monocyotgenes
Published: August 21, 2024
Distribution: Kentucky, New York, Ohio, Pennsylvania,…

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Data last updated: October 19, 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.