Teleflex Medical recalls Rusch EasyCath Kit (ECK120 and ECK125) due to potential non-sterile condition. Affected units may pose infection risks during medical procedures.
Potential for product not to be sterile.
Teleflex Medical is recalling two specific models of Rusch EasyCath Kits because they might not be sterile. This could lead to infections during medical procedures if used improperly.
The kits may not be sterile, which can lead to infections during medical procedures. This happens because the packaging or handling might not maintain sterility standards.
Healthcare professionals and patients using the Rusch EasyCath Kit for medical procedures. Those most at risk are individuals with compromised immune systems or undergoing surgery.
Check for Catalog Numbers ECK120 or ECK125. Lot Numbers 74C1900304 (ECK120) or 74B1901676 (ECK125) with Expiration Dates 03/01/2022 or 06/01/2022.
Verify the Catalog Number and Lot Number on the kit to confirm if it is affected.
The recall is due to potential non-sterile condition, which could lead to infections during medical procedures.
Check the Catalog Number and Lot Number to see if it is affected; if so, contact Teleflex Medical for further instructions.
The recall addresses potential infection risk, not direct injury. The hazard does not involve death or serious injury in normal use.
We’ve drafted a message you can send Teleflex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2086-2019 — Teleflex Medical Teleflex Medical Hello, I own a Teleflex Medical that is covered by recall Z-2086-2019 from Teleflex Medical. 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.