Class I
Medical Device Recall: BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)
Synergetics Inc · June 12, 2024
Reason for Recall
Sterilization certificates could not be validated by the supplier
Distribution
US Nationwide
States Affected
NATIONWIDE
Quantity Affected
2 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2252-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.