95,050 total recalls in our database
Sysco Charlotte
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.
Sysco Charlotte
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.
Sysco Charlotte
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.
Sysco Charlotte
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.
Sysco Charlotte
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.
Sysco Charlotte
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.
Perrigo New York
Failed Degradation/Impurities Specifications: Out of specification related substance results during stability testing.
Failed dissolution specifications
Failed Stability Specification; out of specification (OOS) results for a preservative at 9 month stability study.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Dr. Reddy's Laboratories
Failed Dissolution Specifications: Out of specification results observed for high dissolution.
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.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
Superpotent Drug: product may contain concentrations of oxytocin higher than what is represented on the label.
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.
Failed Impurities/Degradation Specifications: High out of specification results obtained during routine stability testing
Labeling: Incorrect expiration date.
Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.
CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Failed Stability Specification: out of specification results for Sodium Perborate