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 labeling and instruction updates. This recall helps ensure medical devices are used safely during procedures.
The recall involves updating labels and instructions for safe use. Without these updates, there could be confusion about proper device handling during medical procedures.
Healthcare professionals using the specific Palindrome RT Repair Kit models listed in the recall. Patients using these kits during medical procedures are at low risk.
Check for the item code 8888541119 and lot numbers 1708800198, 1714400174, 1904900098, or 2009300086 on the kit packaging.
Look for the item code 8888541119 and specific lot numbers listed in the recall.
No, this recall is for labeling and instruction updates to ensure safe use during medical procedures, not a safety hazard.
Check the item code 8888541119 and lot numbers 1708800198, 1714400174, 1904900098, or 2009300086 on the packaging.
No, the recall does not require stopping use; it involves updating labels and instructions for safe use.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2364-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2364-2021 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.
