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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

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

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 2,021–2,040 of 18,690 recalls

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 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 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 United States Terminated Historical 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 Ongoing Historical 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 Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Rosemary Garlic; NET WT 8 OZ (…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Mild Tandoori; NET WT 8 OZ (22…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Pariva LLC

Product
Pariva Marinated Labneh Bites Za'atar; NET WT 8 OZ (225g); I…
Reason
Product may be contaminated with mold.
Published
August 21, 2024
Distribution
Multiple states

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FDA Recall Terminated Historical recordClass II

Gabapentin Tablets, USP, 600 mg, 500-count bottles, Rx only, Manufactured by: Granules India Limited Hyderabad-500 081, India, Manufactured for: Granules Pharmaceuticals Inc., Chantilly, VA NDC 70010-227-05

by Granules Pharmaceuticals Inc.

Reason
Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Published
August 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles, Packaged By: A-S Medication Solutions, Libertyville, IL 60048. NDC: 50090-5313-2

by A-S Medication Solutions LLC

Reason
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Published
August 14, 2024
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial, For IM or SQ use only, RX only, Compounded by: Empower Pharmacy 7601 N Sam Houston Pkwy W Ste 100, Houston, TX 77064

by EMPOWER CLINIC SERVICES LLC

Reason
Lack of Assurance of Sterility
Published
August 14, 2024
Distribution
Nationwide

View recall →

Data last updated:

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.