Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTSNL) due to potential seal disengagement when mesh products are used incorrectly. Affected units include specific lot numbers and serials.
The potential for trocar seal disengagement when using mesh products incorrectly with the device.
Covidien is recalling its Auto Suture Blunt Tip Trocar (product number OMS-T10BTSNL) because it may disengage when mesh products are used incorrectly. This could lead to improper suturing during medical procedures.
The trocar seal may disengage when mesh products are used incorrectly with the device. This can cause improper suturing during medical procedures, potentially leading to complications.
Medical professionals using the trocar for surgical procedures are most at risk. Patients undergoing surgery with this device may be affected if the seal disengages.
Check for product number OMS-T10BTSNL. Look for specific lot and serial numbers listed in the recall notice: 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.
Verify the product number is OMS-T10BTSNL and check for the listed lot and serial numbers.
The trocar seal may disengage when mesh products are used incorrectly, which could lead to improper suturing during medical procedures.
Check the product number and lot/serial numbers against the list provided in the recall notice. If it matches, contact the manufacturer for further instructions.
The recall notice does not specify a fix or remedy; affected users should check with the manufacturer for guidance.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1467-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1467-2024 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.
