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Percussionaire Corporation recalls High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
Recalled January 24, 2024 · FDA recall Z-0637-2024 · Percussionaire
Hazard
Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user · FDA Class I
Units
2145 units
Sold at
US:AL AR CA CT FL GA IL IN KS LA MI MN MO NC NJ OH OR TN TX UT VA OUS: None
Description
Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user
Product
High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123
Manufacturer(s)
Percussionaire Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →