Covidien recalls specific Palindrome Precision RT Chronic Catheter Kits for updated labeling and instructions to ensure safe use. Affected items include certain lot numbers and item codes.
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 a specific type of chronic catheter kit to add clearer labeling and updated instructions for safe use. This recall helps prevent confusion about proper handling and use of the medical device.
The recall involves updating labels and instructions to improve clarity and safety. The hazard is not a physical risk but a labeling issue that could lead to misunderstandings about proper use.
Healthcare professionals using the specific catheter kit model described in the recall are most likely affected. Patients using this device are not directly at risk from the recall itself.
Check for the item code 8888541044P on the kit. Affected lots include 1729700119, 18177: 1810400147, 1828900137, 2014900148, 2014900151, 2034400131.
Check for updated labeling and instructions on the device as part of the recall process.
The recall is to implement point-of-use labeling and enhance the Instructions for Use to ensure safer handling and use of the catheter kit.
Review the labeling and instructions for updates; no immediate action is required beyond checking for the new information.
Yes, affected lot numbers include 1729700119, 1817700205, 1910600266, 2014900148, 1810400147, 1828900137, 2014900151, and 2034400131.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2374-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2374-2021 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.
