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Synergetics Inc recalls BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Recalled July 17, 2024 · FDA recall Z-2251-2024 · Synergetics
Hazard
Sterilization certificates could not be validated by the supplier · FDA Class I
Units
14 units
Sold at
US Nationwide
Description
Sterilization certificates could not be validated by the supplier
Product
BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)
Manufacturer(s)
Synergetics Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →