165 FDA recalls mention Magnesium. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Magnesium.
Reason Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Reason CGMP Deviations: Failure to properly investigate failed microbial testing.
Reason CGMP Deviations: Failure to properly investigate failed microbial testing.
Reason Microbial Contamination of Non-Sterile Products
Reason Microbial Contamination of Non-Sterile Products
Reason CGMP Deviations
Reason CGMP Deviations
Reason cGMP deviations
Reason cGMP deviations
Reason cGMP deviations
Reason cGMP deviations
Reason CGMP Deviations: Customer complaint for the presence of a staple co-mingled with capsules within the bottle.
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason Temperature Abuse: Product exposed to temperature outside specified limits.
Reason CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Reason Cross- contamination with other products: The excipient, Crospovidone, NF is contaminated with theophylline
Reason Cross- contamination with other products: The excipient, Crospovidone, NF is contaminated with theophylline
Reason Cross- contamination with other products: The excipient, Crospovidone, NF is contaminated with theophylline
Reason Discoloration: product contains brown pellets
Reason Lack of Assurance of Sterility
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