Covidien recalls specific Palindrome RT Repair Kit models for updated labeling and instructions to ensure safe use. Affected items include Lot Numbers 1704700210, 1822600138, and 1826200177.
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 to add clearer labels and updated instructions. This helps users follow safety guidelines properly without causing harm.
The recall involves updating labels and instructions to improve clarity and safety. Without these updates, users might not follow procedures correctly, but the hazard is not severe.
Healthcare professionals using the Palindrome RT Repair Kit for medical procedures are most likely affected. The recall targets specific lot numbers sold for sterile use.
Check the item code 8888541144 and lot numbers 1704700210, 1822600138, or 1826200177. The product is a sterile medical repair kit sold for specific procedures.
Look for the item code 8888541144 and lot numbers listed in the recall.
Covidien is updating labels and instructions to ensure safer use without causing harm.
Check the item code and lot numbers to see if it's affected; no action is needed if it's not listed.
The recall is for labeling and instructions, not a safety hazard, so no injury risk is expected.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2368-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2368-2021 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.
