Covidien recalls specific Palindrome RT Repair Kit models for updated labeling and instructions to ensure safe use during medical procedures.
This voluntary withdrawal is being conducted to implement point-of-use labeling on each device and enhancements to the Instructions for Use (IFU).
Covidien is recalling certain Palindrome RT Repair Kits due to a need for updated labeling and instructions. This recall helps ensure safe use during medical procedures without immediate safety risks.
The recall involves updating labeling and instructions for safe use. The hazard is not a physical risk but a need for clearer guidance to prevent misuse during medical procedures.
Healthcare professionals using the specific Palindrome RT Repair Kit models listed. Those most at risk are medical staff handling these kits during procedures.
Check for the item code 8888541128 and lot numbers listed: 1834500202, 1920500219, 2014900143, 2020400107, 1914800210, 2009300121, 2017500133, 2023300110.
Look for the item code 8888541128 and lot numbers listed in the recall notice.
Covidien is recalling these kits to implement updated labeling and instructions for safe use during medical procedures.
No, the recall is for updated labeling and instructions, not an immediate safety hazard.
Check the product label for the item code and lot numbers; no action is needed beyond verifying the model.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2366-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2366-2021 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.