Home / Recalls / Medical Devices
Percussionaire Corporation recalls Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Recalled January 24, 2024 · FDA recall Z-0693-2024 · Percussionaire
Hazard
Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy. · FDA Class I
Units
195
Sold at
US: RI, CA, TX
Description
Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy.
Product
Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)
Manufacturer(s)
Percussionaire Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →