Hydrogen Peroxide 16 fl. oz. and 32 oz. bottles distributed to…
CGMP Deviations: product held outside appropriate storage temperature conditions.
2,357 recalls · Class II, newest first
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
CGMP Deviations: product held outside appropriate storage temperature conditions.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
cGMP deviations: product stored outside of labeled temperature requirements.
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Subpotent Drug: FDA analysis has revealed some bottles of these products were sub potent for ethanol.
Defective Delivery System: customer complaints exceeded respective action limits.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Marketed Without an Approved NDA/ANDA
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
CGMP Deviations