Skip to main content

Data Explorer

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.

37,135
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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.

Filters
Recall details
Location
Date range
Sort results
Clear filters
Metric
View
Recalls announced by month (Year to date)

A chart of recalls grouped by month.

Download CSV

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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 11,061–11,080 of 20,519 recalls

FDA Recall Terminated Historical recordClass II

Moisturizing Lubricant Eye Drops, 0.25% Sodium Carboxymethylcellulose, 0.5 Fl OZ (15mL) Distributed by: Walgreen Co, 200 Wilmont Rd Deerfield IL 60015 NDC 00363-9651-01.

by Akorn Inc

Reason
Failed Stability Specification: out of specification results for Sodium Perborate
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-09

by ICU Medical Inc

Reason
CGMP Deviations
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Ephedrine Sulfate, 50 mg/10 mL, 10 mL Single Use Syringe, Rx only, US Compounding Pharmacy 1270 Don's Lane Conway, AR 800-718-3588, Barcode: 62295308407

by US Compounding Inc

Reason
Lack of assurance of sterility.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 India NDC 55111-533-01

by Dr. Reddy's Laboratories, Inc.

Reason
Failed Dissolution Specifications: Out of specification results observed for high dissolution.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP 50 mg/12.5 mg, a) 90-count bottle (NDC: 13668-116-90), b) 1000-count bottle (NDC: 13668-116-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM and HYDROCHLOROTHIAZIDE TABLETS, USP, 100 mg/12.5 mg, a) 90-count bottle (NDC: 13668-117-90), b) 1000-count bottle (NDC: 13668-117-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 25 mg, 90-count bottle (NDC: 13668-113-90), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count bottle (NDC: 13668-409-30), b) 90-count bottle (NDC: 13668-409-90), c) 1000-count bottle (NDC: 13668-409-10), Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 30-count (NDC: 13668-115-30), b) 90-count (NDC: 13668-115-90), c) 1000-count (NDC: 13668-115-10) per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana Inda

by Torrent Pharma Inc.

Reason
CGMP Deviations: FDA lab confirmed presence an impurity, N-nitrosodimethylamine (NDEA) contained in the API used to manufacture the product above the interim acceptable daily intake level of 0.083 parts per million.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Oxytocin 30 Units added to NS 500 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 503 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-706-50.

by Advanced Pharma Inc.

Reason
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Oxytocin 20 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1002 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-703-99.

by Advanced Pharma Inc.

Reason
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Oxytocin 10 Units added to NS 1000 mL (oxytocin and 0.9% Sodium Chloride) Injectable Solution, Approximately 1001 mL Sterile single use bag, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, NDC 42852-730-99.

by Advanced Pharma Inc.

Reason
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Published
February 27, 2019
Distribution
Nationwide

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
YOGURT VAN W/M&M¿
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
Yoplait YOGURT STRAW/STRAW BAN LT CUP
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
Dannon YOGURT PLAIN LOW FAT
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
Yoplait YOGURT PEACH ORIGINAL
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
GFGB SAUCE TARTAR
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
Sysco Classic SALAD MACARONI CLASSIC
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
IMPFRSH ONION RED DICED FRSH 1/4 IN¿
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

View recall →

FDA Recall United States Completed Historical recordClass II

Sysco Charlotte

Product
Simply Lemonade LEMONADE FRESH PLS BTL
Reason
The firm discovered that one of their coolers malfunctioned and the food was not held at an appropriate temperature. Because the holding temperature could affect food safety, this food could be unsafe for consumption.
Published
February 27, 2019
Distribution
Product was shipped to GA, NC & SC.

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.