Covidien recalls specific Palindrome Precision RT Chronic Catheter Kits for updated labeling and instructions to improve safety.
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 Precision RT Chronic Catheter Kits with symmetrical tips. This recall involves updating labels and instructions to ensure safer use during medical procedures.
The recall is for implementing updated labeling and instructions for safe use. This change addresses potential confusion in medical procedures by providing clearer guidance without altering the device's function.
Healthcare professionals using the specific catheter kits with the listed lot numbers are affected. Patients receiving these catheters are at minimal risk due to the labeling update being a procedural improvement.
Check for the product name 'Palindrome Precision RT Chronic Catheter Kit Symmetrical Tip, Reverse-Tunneled 15 Fr/Ch (5.0 mm) x 23 cm' and the listed lot numbers on the packaging.
Look for the item code 8888541023P and the specific lot numbers listed in the recall notice.
The recall is to implement updated labeling and instructions for safer medical use without changing the device's function.
No, the recall does not require stopping use; it involves updating labels and instructions for safer procedures.
Check the item code 8888541023P and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2371-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2371-2021 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.