Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in… — Class II medical device recall Z-2336-2024
Ongoing recall by MICROspecialties, Inc., reported 2024-07-17, distributed in MO. Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative
| Recall number | Z-2336-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MICROspecialties, Inc., Middletown, CT, United States |
| Recall initiated | 2024-06-05 |
| Classified | 2024-07-11 |
| Reported by FDA | 2024-07-17 |
| Distributed | MO |
| Quantity | 804 units |
| UPC / GTIN / UDI-DI | 10841305101132 |
| Lot numbers | P62764970R |
| Model numbers | 18069W |
Product
Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069W
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2336-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.