FDA Device recall Z-0663-2025
Microscissor Tip (Disposable)
- FDA Device
- Class II
- ongoing
- Published 2024-12-18
On 2024-12-18 the FDA classified a Class II recall of Microscissor Tip (Disposable) by Microline Surgical, citing A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0663-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-11-05 |
| Published | 2024-12-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Microline Surgical |
| Distribution | US |
Product
Microscissor Tip (Disposable); Microline Catalog #: 3122.
Reason
A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of the heat shrink breaking off.
Identifiers
| code_info | Microline Catalog #: 3122; UDI/DI: 811099010036; Lot Number: 00172110. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0663-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.