Covidien recalls Auto Suture Blunt Tip Trocar (OMS-T10BTS) due to potential seal disengagement when used incorrectly with mesh products. Affected units include specific lot numbers.
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-T10BTS because they may disengage when used incorrectly with mesh products. This could lead to improper closure of surgical wounds. Consumers should check their device for the listed lot numbers and contact the manufacturer for guidance.
The trocar seal may disengage if the device is used incorrectly with mesh products, potentially causing the surgical wound to not close properly. This could lead to complications like infection or excessive bleeding.
Medical professionals using the device during surgeries are most at risk. Patients who have received the device for procedures may also be affected if the device is used incorrectly.
Check the product number on the device, which is OMS-T10BTS. Look for the specific lot numbers listed in the recall notice, such as P1D1416, P1E1509, and others.
Look for the lot numbers listed in the recall notice, such as P1D1416, P1E1509, or others.
The recall states the hazard occurs when used incorrectly with mesh products. If used properly, the risk is low.
Check the lot number on your device against the list provided in the recall notice. Contact Covidien for further guidance.
Yes, the product number OMS-T10BTS with specific lot numbers listed in the recall notice are affected.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1469-2024 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1469-2024 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.
