Covidien is a leading manufacturer of medical devices and healthcare products. We provide innovative solutions for healthcare professionals and patients worldwide.
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 a leading manufacturer of medical devices and healthcare products. We provide innovative solutions for healthcare professionals and patients worldwide.
Covidien is a reputable medical device manufacturer with a long history of providing safe and effective products. The risk associated with their products is considered low due to rigorous quality control and regulatory compliance.
All healthcare professionals and patients
Ensure that the medical devices purchased from Covidien are certified by relevant regulatory bodies such as the FDA, CE, or other international standards.
Verify the product's certification status with the relevant regulatory authority (e.g., FDA for the US, CE for the EU).
Check the product's expiration date and ensure it is within the valid period.
Ensure that the product is used according to the manufacturer's instructions for use.
Yes, Covidien is a reputable medical device manufacturer with a long history of providing safe and effective products. The risk associated with their products is considered low due to rigorous quality control and regulatory compliance.
Ensure that the medical devices purchased from Covidien are certified by relevant regulatory bodies such as the FDA, CE, or other international standards.
Contact the manufacturer directly or reach out to your healthcare provider for assistance.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1320-2022 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1320-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
