Covidien recalls specific Palindrome RT Chronic Catheter Kits for updated labeling and instructions to improve safety and use.
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 tip design. This recall involves updating labels and instructions to ensure safer use during medical procedures.
The recall is for adding point-of-use labeling and improving Instructions for Use (IFU) to enhance safety. This update addresses potential confusion in medical procedures without immediate safety risks.
Healthcare professionals using the specific catheter kits listed in the recall. Patients receiving these catheters are at minimal risk due to the labeling update focus.
Check for the item code 8888541028 and lot numbers listed: 1726500092, 1806600073, 1833800146, 2009200089, 1728600060, 1815800078, 1904900089, 2012100138, 1733300161, 1816400084, 1906300059, 2020400105, 1733700172, 1826200176, 1910200093, 2026000059, 1733700178, 1826800155, 1917600105, 2027200241, 1800300143, 1828200124, 1926100255, 2028200207, 1804000125, 1831000115, 1931600120, 2028200207, 1804500144, 1832300108, 2000700070.
Identify the item code 8888541028 and lot numbers listed in the recall notice.
To implement point-of-use labeling and enhance Instructions for Use (IFU) for safer medical procedures.
Check the item code and lot numbers to see if it's affected; no action is needed beyond verifying the product details.
The recall focuses on labeling and instructions, not immediate safety risks, so the risk is low.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2360-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2360-2021 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.
