FDA Closes Recall of American Regent Cyanocobalamin Injection Over Particulate Contamination
The FDA has closed the Class II recall of certain cyanocobalamin injection vials, confirming the action is complete.
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The FDA has closed the Class II recall of certain cyanocobalamin injection vials, confirming the action is complete.
FDA classifies recall of 169,200 vials as Class II due to hair, glass, and paraformaldehyde particles.
American Regent, Inc. recalls 86,100 vials of Papaverine HCl Injection due to particulate matter contamination.
FDA Class II recall of 316,450 vials due to hair, glass, and paraformaldehyde particles.
FDA Class II recall of 89,775 vials of atropine sulfate injection after contamination with hair, glass, and paraformaldehyde was identified.
FDA classifies recall of 98,200 vials as Class II due to hair, glass, and paraformaldehyde particles.
FDA Class II recall of 185,775 vials of Multrys Trace Elements Injection 4, USP, due to particulate matter identified as hair, glass and/or paraformaldehyde.