Class I

Medical Device Recall: BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, 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

116 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2253-2024

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.

Synergetics Inc Medical Device Recall: BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye) | SafeCheck