FDA Device recall Z-1467-2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTSNL
- FDA Device
- Class II
- ongoing
- Published 2024-04-10
On 2024-04-10 the FDA classified a Class II recall of Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTSNL by Covidien, citing the potential for trocar seal disengagement when using mesh products incorrectly with the device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1467-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-02-28 |
| Published | 2024-04-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Covidien |
| Distribution | US |
Product
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTSNL
Reason
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Identifiers
| code_info | Product Number/CFN: OMS-T10BTSNL; UDI/DI: 10884521539648; Lot Serial Number: P0M1930, P1C1684, P1C1685, P1D1418, P1F154…Product Number/CFN: OMS-T10BTSNL; UDI/DI: 10884521539648; Lot Serial Number: P0M1930, P1C1684, P1C1685, P1D1418, P1F1548, P1F1549, P1J0729, P1J1343, P1K0356, P1M0969, P2A0779, P2B0758, P2D0021, P2D0022, P2D0023, P2F0324, P2H0410, P2H0411, P2J0053, P2J0456, P2L0093, P2M0416, P2M0417, P3C0354, P3E0462; |
|---|
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-1467-2024%22
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