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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
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 1,961–1,980 of 18,376 recalls

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 I

Foppen Paling En Zalm B.V.

Product
Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged…
Reason
Potential contamination with Listeria monocytogenes
Published
August 21, 2024
Distribution
AL, AR, GA, IL, IN, KY, LA, MI, MO, MS,…

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FDA Recall United States Terminated Historical 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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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Poblano packaged as 5lb half sliced with 2 bags per case, 5l…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Jalapeno peppers packaged as 5lb diced with 2 bags per case,…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Green Peppers packaged in plastic bags cont…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Green Beans packaged in plastic bags at 1lb…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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FDA Recall United States Terminated Historical recordClass I

RS Hanline and Company Inc

Product
Freshire Farms - Jalapenos packaged in plastic bags at 8oz,…
Reason
Potential contamination with Listeria monocyotgenes
Published
August 21, 2024
Distribution
Kentucky, New York, Ohio, Pennsylvania,…

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.