FDA Device recall Z-0486-2026
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin)
- FDA Device
- Class II
- ongoing
- Published 2025-11-19
On 2025-11-19 the FDA classified a Class II recall of Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin) by Covidien, citing A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0486-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-25 |
| Published | 2025-11-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Covidien |
| Distribution | US |
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
Reason
A manufacturing issue could lead to a malformed cover tube press which can lead to internal components' movement during firing - leading to the potential for uncontrolled motion.
Identifiers
| code_info | CFN: BOX06170V4; UDI-DI: 00763000988975; Lot numbers: 0231961695; |
|---|
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-0486-2026%22
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