Covidien recalls specific Palindrome RT Chronic Catheter Kits for updated labeling and instructions to improve safety and usage clarity.
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 Chronic Catheter Kits with symmetrical tips. This recall involves updating labels and instructions to ensure safer use and better clarity for healthcare providers.
The recall focuses on adding clearer labels and updated instructions for safe use. This helps prevent confusion and ensures proper handling of the catheter kits during medical procedures.
Healthcare professionals using the specific Palindrome RT Chronic Catheter Kits with symmetrical tips are likely affected. Those in medical settings handling these kits are at the highest risk.
Check for the item code 8888541023 and lot numbers listed in the recall notice. These kits were sold with specific lot numbers between 2017 and 2027.
Look for the item code 8888541023 and lot numbers listed in the recall notice.
The recall is for implementing updated labeling and instructions to improve safety and clarity for healthcare providers.
No, the recall does not require stopping use but involves updating labels and instructions.
Check the item code and lot numbers to confirm if your product is affected; no action is needed beyond checking labels.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2359-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2359-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
