FDAAugust 29, 2022device
Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Incidents of device splitting or detaching during use
What to do
FDA enforcement status: Ongoing
Brands named
teleflex
UPCs
040267044004780402670434800804026704400485
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820552023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820502023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800952023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800552023-05-25
- FDARUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 1124800302023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120801002023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820902023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820602023-05-25
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