FDAAugust 26, 2016device
Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tracheostoma and narrow-lumen tracheas. When using cannulas with curr. For short term intermittent inflation.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The connector may disconnect from the tracheostomy tube during use.
What to do
FDA enforcement status: Terminated
Brands named
teleflex medicalteleflex
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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