Teleflex recalls Iso-Gard Filter S, Tethered Cap models 19211T and 19212T (US only) due to incidents of device splitting or detaching during use. No remedy specified in official notice.
Incidents of device splitting or detaching during use
Teleflex is recalling certain Iso-Gard Filter S, Tethered Cap medical gas filters (models 19211T and 19212T) sold in the U.S. because they can split or detach during use. This could lead to improper gas flow in medical settings.
The filters can split or detach during use, potentially causing improper gas flow in medical systems. This could lead to inadequate oxygen delivery or other medical gas issues for patients.
Healthcare facilities and medical professionals using these filters in oxygen or gas delivery systems. Patients receiving medical gas treatment are at risk if the filter detaches.
Check for model numbers 19211T or 19212T on the filter. These are single-use microbial medical gas filters sold in the U.S. The unique identifiers (UDI) listed in the recall notice can help identify affected units.
Look for model numbers 19211T or 19212T on the filter.
The recall is for incidents of device splitting or detaching during use, which could cause improper gas flow in medical systems.
Check for model numbers 19211T or 19212T. The unique identifiers (UDI) listed in the recall notice can help identify affected units.
The official notice does not specify a remedy, so contact Teleflex directly for guidance.
We’ve drafted a message you can send Teleflex to request your refund or repair — edit it as you like.
Subject: Recall Z-0074-2023 — Teleflex Teleflex Hello, I own a Teleflex that is covered by recall Z-0074-2023 from Teleflex. 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.