Synergetics Inc: Device Recall

Recall #Z-2251-2024 · 06/12/2024

Class I: Dangerous

Recall Details

Recall Number: Z-2251-2024
Classification: Class I
Product Type: Device
Recalling Firm: Synergetics Inc
Status: Ongoing
Date Initiated: 06/12/2024
Location: O Fallon, MO, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 14 units

Reason for Recall

Sterilization certificates could not be validated by the supplier

Product Description

BAUSCH+LOMB, I-PACK Injection Kit, REF 18060, for the administration of intravitreal injection (eye)

Distribution Pattern

US Nationwide

Other Recalls by Synergetics Inc

Class I: Dangerous 06/12/2024

Sterilization certificates could not be validated by the supplier
Class I: Dangerous 06/12/2024

Sterilization certificates could not be validated by the supplier
Class I: Dangerous 06/12/2024

Sterilization certificates could not be validated by the supplier

View all recalls by Synergetics Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.