Covidien recalls specific Palindrome H Chronic Catheters for possible fluid leaks during hemodialysis use. Affected units have model numbers starting with 8888145043 or 8888145044. Contact for replacement.
There is a potential leaking condition within the hub of specific chronic dialysis catheters, due to an inter-lumen void in the hub component, which may result in unanticipated fluid return during use.
Covidien is recalling certain Palindrome H Chronic Catheters used in hemodialysis due to a potential leak in the hub component. This leak could cause unanticipated fluid return during use, which may lead to complications for patients.
The hub component of specific Palindrome H Chronic Catheters has an inter-lumen void that can cause fluid to leak unexpectedly during use. This may result in unanticipated fluid return, potentially causing complications for patients receiving dialysis or infusion treatments.
Patients using hemodialysis or apheresis treatments with the recalled catheters are most at risk. Healthcare providers who use these catheters for infusion therapy may also be affected.
Check for model numbers starting with 8888145043 or 8888145044 on the catheter packaging or label. The serial number and GTIN are listed in the recall notice for specific units.
Look for model numbers starting with 8888145043 or 8888145044 on the catheter packaging or label.
Reach out to Covidien for guidance on replacement or return options for affected units.
Covidien recalls specific Palindrome H Chronic Catheters due to a potential leak in the hub component that could cause unanticipated fluid return during use.
Model numbers starting with 8888145043 or 8888145044 are affected, as listed in the recall notice.
No, but you should check if your catheter is affected and contact Covidien for guidance on next steps.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1317-2022 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1317-2022 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.
