Natrum Phosphoricum 6X Tablets
CGMP Deviations: products were not manufactured under current good manufacturing practices.
1,586 recalls · Class II, newest first
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: products were not manufactured under current good manufacturing practices.
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in Ranitidine tablets, capsules and syrups.
CGMP Deviations: Presence of NDMA impurity detected in product.
CGMP Deviations: Presence of NDMA impurity detected in product.
Presence of foreign substance: Brown/black particles found during stability testing.
CGMP Deviations: Presence of NDMA impurity detected in product.
Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Microbial contamination of non-sterile product.
Failed Stability Specifications: Product exceeds compendia and firm's specifications for iron content.
CGMP Deviations: Presence of NDMA impurity detected in product.
CGMP Deviations: Presence of NDMA impurity detected in product.