Covidien recalls specific Palindrome RT Repair Kit 15 FR TAL 33cm sterile kits for updated labeling and instructions. No immediate safety risk but requires attention to ensure proper 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 a specific type of sterile surgical repair kit for updated labeling and instructions. This recall does not pose a safety risk but ensures users follow the latest guidelines for proper use.
The recall involves updating labeling and instructions for proper use. The hazard is not a safety risk but ensures users follow the latest guidelines to avoid potential misuse.
Healthcare professionals using the Palindrome RT Repair Kit 15 FR TAL 33cm sterile kit with item code 8888541133 are affected. Those most at risk are users who may not have the updated labeling or instructions.
Check for the item code 8888541133 on the kit. The recall applies to specific lot numbers starting with 1705400292.
Check the kit for updated labeling and instructions to ensure proper use.
No, this recall is for updated labeling and instructions, not a safety hazard.
Review the updated labeling and instructions to ensure proper use; no action is needed beyond this.
Look for item code 8888541133 and lot numbers starting with 1705400292.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-2367-2021 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-2367-2021 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.
