Microscissor Tip — Class II medical device recall Z-0663-2025
Ongoing recall by Microline Surgical, Inc., reported 2024-12-18, distributed nationwide. A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
| Recall number | Z-0663-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microline Surgical, Inc., Beverly, MA, United States |
| Recall initiated | 2024-11-05 |
| Classified | 2024-12-10 |
| Reported by FDA | 2024-12-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP |
| Quantity | 200 units |
| UPC / GTIN / UDI-DI | 00811099010036 |
| Lot numbers | 00172110 |
| Model numbers | 3122 |
Product
Microscissor Tip (Disposable); Microline Catalog #: 3122.
Reason for recall
A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
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-0663-2025. 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.