Magnesium Hydroxide 1200 mg
Microbial Contamination of Non-Sterile Products.
14,806 recalls, newest first
Microbial Contamination of Non-Sterile Products.
Microbial Contamination of Non-Sterile Products.
Microbial Contamination of Non-Sterile Products
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.
Failed Tablet/Capsule Specification; oversized tablet found in a bottle
CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification for impurities.
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the product to contain undeclared diclofenac.
Microbial contamination of non-sterile product.
Microbial contamination of non-sterile product.
Microbial contamination of non-sterile product.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Superpotent: High Out of specification (OOS) test result for percent label claim (%LC).
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Lack of Assurance of Sterility