Class II — MICROspecialties, Inc.
| Recalling firm | MICROSPECIALTIES LLC |
|---|---|
| Registered facility | Microspecialties LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection. |
| Product | Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060 |
| Quantity | 2316 units |
| Distribution | MO |
| Initiated | 2024-06-05 |
| Classified | 2024-07-11 |
| Recall number | Z-2333-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MICROspecialties, Inc. (Z-2333-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94794/
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