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Synergetics Inc FDA Recalls
4 recalls on file across devices, 4 of them Class I and 4 still open. This firm is not matched to a listed company.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| BAUSCH+LOMB, I-PACK Injection Kit with Wire Speculum, REF 18069W, for the administration of intravitreal injection (eyeClass IJun 12, 2024Sterilization certificates could not be validated by the sup |
| BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)Class IJun 12, 2024Sterilization certificates could not be validated by the sup |
| BAUSCH+LOMB, I-PACK Injection Kit with Drape, REF 18061, for the administration of intravitreal injection (eye)Class IJun 12, 2024Sterilization certificates could not be validated by the sup |
| BAUSCH+LOMB, I-PACK Injection Kit Custom, REF 18069, for the administration of intravitreal injection (eye)Class IJun 12, 2024Sterilization certificates could not be validated by the sup |