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Teleflex Medical recalls Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow t
Recalled October 26, 2016 · FDA recall Z-0044-2017 · Teleflex Medical
Hazard
The connector may disconnect from the tracheostomy tube during use. · FDA Class I
Units
1095 units
Sold at
Worldwide Distribution: US (nationwide) to CA and countries of: Austria, Belgium, France, Germany, Italy, Japan, Poland, and Turkey.
Description
The connector may disconnect from the tracheostomy tube during use.
Product
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.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →