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DRE Medical Group Inc recalls Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predeter
Recalled July 5, 2023 · FDA recall Z-2025-2023 · DRE Medical Group
Hazard
Devices were imported with Japanese Language and NIST Oxygen Gas Fittings and retrofitted, may pose a serious health risk as the gas pathway of these devices may be contaminated. · FDA Class II
Units
22 units
Sold at
US: CA, FL
Description
Devices were imported with Japanese Language and NIST Oxygen Gas Fittings and retrofitted, may pose a serious health risk as the gas pathway of these devices may be contaminated.
Product
Philips Respironics V60 Ventilator-Intended to mechanically control or assist patient breathing by delivering a predetermined percentage of oxygen in the breathing gas. Model Number: R1053618 and R1076709. These are retrofitted device.
Manufacturer(s)
DRE Medical Group Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →