MICROspecialties, Inc.: Device Recall

Recall #Z-2334-2024 · 06/05/2024

Class II: Risk

Recall Details

Recall Number: Z-2334-2024
Classification: Class II
Product Type: Device
Recalling Firm: MICROspecialties, Inc.
Status: Ongoing
Date Initiated: 06/05/2024
Location: Middletown, CT, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 96 units

Reason for Recall

Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.

Product Description

Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061

Distribution Pattern

Other Recalls by MICROspecialties, Inc.

Class II: Risk 06/05/2024

Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
Class II: Risk 06/05/2024

Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
Class II: Risk 06/05/2024

Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.

View all recalls by MICROspecialties, 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.