95,064 total recalls in our database
McCain Foods USA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
Potential foreign object; plastic and rubber pieces.
McCain Foods USA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
McCain Foods USA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
McCain Foods USA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
McCain Foods USA
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
Defective Container: Repetitive complaints received indicating pump not working.
Failed Impurities/Degradation Specifications:Out of specification result noticed for total impurities observed during stability analysis
Valeant Pharmaceuticals North America
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.
Lack of assurance of sterility: loss of container integrity.
Heritage Pharmaceuticals
Lack of Assurance of Sterility: complaints received about dried powder on the outside of the bottle
Subpotent drug: During testing of the retention sample, the firm discovered that the product was sub-potent.
Westlab Pharmacy, Inc.
Lack of Process Controls
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.
Valeant Pharmaceuticals North America
CGMP deviations: Notice received from supplier of a voluntary recall of all their nasal products and baby oral gels due to the possibility of microbial contamination. No positive results for the firm's products. were obtained. After the firm review, cGMP deviations ere evident.
Failed dissolution specifications: Out-of-Specification dissolution test result obtained during routine stability testing.
Lack of Process Controls
Defective Delivery System: There is a potential for some tablets to be missing the laser drilling which might affect drug release.