Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BT) due to potential seal disengagement when used incorrectly with mesh products. Affected units have specific lot numbers. Stop using immediately if you have this device.
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Covidien is recalling Auto Suture Blunt Tip Trocar devices (product number OMS-T10BT) because they can disengage when used incorrectly with mesh products. This could lead to improper sealing during medical procedures. If you own this device, stop using it immediately and contact Covidien for instructions.
The trocar seal may disengage when the device is used incorrectly with mesh products. This could cause improper sealing during medical procedures, potentially leading to complications like leaks or infections.
Medical professionals who use this device during surgeries are most at risk. Patients undergoing procedures with this device may also be affected if the seal disengages.
Check for product number OMS-T10BT on the device. Look for lot/serial numbers listed in the recall notice: P1D1353, P1D1355, P1D1409, P1D1410, P1D1506, P1D1507, P1E1402, P1E1403, P1E1505, P1E1506, P1F0061, P1F0062, P1F0063, P1F1018, P1F1019, P1F1388, P1F1546, P1G0140, P1G1117, P1G1119, P1G1121, P1G1364, P1H0049, P1H0421, P1H0527Q, P1H0859, P1H0860, P1J1272, P1J1321, P1J1339, P1J1342, P1K0179, P1K0180, P1K0182, P1K0353, P1K0560, P1K0561, P1K0589, P1L0490, P1L0681, P1L0705, P1L0976, P1M0021, P1M0022, P1M0744, P1M0745, P1M0970, P1M0971, P1M1151, P1M1152, P2A0118, P2B0028Q, P2B0137, P2B0139, P2B0308, P2B0745, P2B0912, P2B0913, P2C0175, P2C0178, P2C0643, P2C0758, P2C0764, P2C0765, P2C0877, P2C0878, P2D0231, P2D0232, P2D0373, P2D0374, P2D0415, P2D0539, P2D0540, P2E0244, P2E0245, P2E0371, P2F0041, P2F0042, P2F0133, P2F0134, P2F0135, P2F0449, P2F0450, P2F0451, P2F0452, P2F0453, P2F0454, P2G0141Q, P2G0533, P2H0085, P2H0142, P2H0419, P2H0570, P2J0081, P2J0362, P2J0442, P2J0443, P2J0460, P2K0080, P2K0123, P2K0432, P2K0565, P2L0554, P2L0555, P2L0556, P2M0032, P2M0408, P2M0409, P2M0410, P2M0411, P3A0084, P3A0085, P3A0086, P3A0087, P3A0271, P3A0272, P3A0273, P3A0277, P3A0278, P3A0279, P3B0075, P3B0147, P3B0158, P3B0162Q, P3D0121, P3D0122, P3D0150, P3D0151, P3D0152, P3D0399, P3D0400, P3D0401, P3E0294, P3E0295, P3E0315, P3E0369, P3F0461, P3F0462, P3H1033, P3H1034, P3H1193, P3H1194, P3H1195, P3J0855, P3J0856, P3J0857, P3J1100, P3J1101, P3J1102, P3J1103, P3K0951, P3K1067, P3K1068, P3K1069, P3K1243, P3K1244, P3K1339, P3K1340, P3L0889, P3L0890.
If you have the recalled Auto Suture Blunt Tip Trocar (product number OMS-T10BT), stop using it right away.
The product number is OMS-T10BT.
Check for product number OMS-T10BT and look for the specific lot/serial numbers listed in the recall notice.
Stop using it immediately and contact Covidien for instructions on how to return or replace it.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1470-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1470-2024 from Covidien. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
