Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTNL) 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 Auto Suture Blunt Tip Trocar devices with product number OMS-T10BTNL because they can become disengaged when used incorrectly with mesh products. This could lead to improper closure of surgical wounds.
The trocar seal can become disengaged when the device is used incorrectly with mesh products. This may cause the device to fail to properly close surgical wounds, potentially leading to complications.
Medical professionals who use this device 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-T10BTNL on the device. Look for specific lot and serial numbers listed in the recall notice, which include many combinations starting with P0L1440 through P3L0892.
Identify the product number (OMS-T10BTNL) and lot/serial numbers listed in the recall notice.
The recall states that the device may disengage when used incorrectly with mesh products, so it is not safe to use without checking the recall details.
Check for product number OMS-T10BTNL and specific lot/serial numbers listed in the recall notice, which include many combinations starting with P0L1440 through P3L0892.
The recall does not specify a remedy, so contact the manufacturer for guidance on whether to stop using the device or take other steps.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1466-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1466-2024 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.
