FDA Device recall Z-1468-2024
Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T12BT
- 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-T12BT 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-1468-2024 |
| 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-T12BT
Reason
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Identifiers
| code_info | Product Number/CFN: OMS-T12BT; UDI/DI: 20884521081090, 10884521081093; Lot Serial Number: P1C1924, P1D0400, P1D0400, P1…Product Number/CFN: OMS-T12BT; UDI/DI: 20884521081090, 10884521081093; Lot Serial Number: P1C1924, P1D0400, P1D0400, P1D1411, P1D1412, P1D1508, P1F1483, P1F1484, P1F1484, P1F1485, P1F1485, P1F1591, P1G0141, P1G0141, P1G1118, P1G1120, P1H0046, P1H0046, P1H0047, P1H0047, P1H0048, P1H0048, P1H0861, P1H0861, P1H0862, P1H0862, P1J0858, P1J0858, P1J0860, P1J0860, P1K0455, P1K0455, P1K0838, P1K1052, P1L0926, P1L0926, P1L0985, P1M0026, P1M0026, P1M0027, P1M0027, P1M0028, P1M0028, P1M0031, P1M0031, P1M0743, P1M0743, P2A0129, P2A0744, P2A0744, P2A0745, P2B0746, P2B0746, P2C0176, P2C0176, P2C0177, P2C0177, P2C0230, P2C0230, P2C0231, P2C0231, P2C0232, P2C0232, P2C0233, P2C0233, P2C0879, P2C0879, P2D0512, P2D0512, P2E0351, P2E0351, P2E0370Q, P2E0664, P2E0664, P2F0486, P2F0486, P2G0305, P2G0305, P2H0086, P2H0086, P2H0087, P2H0148, P2H0148, P2H0308, P2H0409, P2H0415, P2H0415, P2H0579, P2H0579, P2J0008, P2J0008, P2J0082, P2J0082, P2J0458, P2J0459, P2J0459, P2K0081, P2K0081, P2K0124, P2K0124, P2K0435, |
|---|
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-1468-2024%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.