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Serious recall: Injury is possible or has been reported. Take action promptly.

Covidien, LP 2024-04-10 Health serious FDA
Health · FDA · Recall #FDA-Z-1470-2024

Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BT Recall

Issued April 10, 2024 · Covidien, LP

In April 2024, Covidien, LP recalled the Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BT, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

The potential for trocar seal disengagement when using mesh products incorrectly with the device.

What you should do

  1. 1 Stop using Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BT right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Covidien, LP to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Covidien, LP
Category
Health
Recall date
April 10, 2024
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Aruba, Australia, Austria, Belgium, Brazil, Bulgaria, Canada,
Recall number
FDA-Z-1470-2024
Made in
United States
Issuing agency
FDA

In context

  • Covidien, LP has 5 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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