Hidrex Recalls
3 recalls on record · March 1, 2017 to March 1, 2017 · Medical Devices
March 1, 2017Medical DevicesFDA
Hidrex GmbH recalls Daavlin Aquex (DAAV1000)
Hazard: The device was reclassified from a class III device to a class II device and there are new documentation requirements.
March 1, 2017Medical DevicesFDA
Hidrex GmbH recalls Hidrex USA DVP1000
Hazard: The device was reclassified from a class III device to a class II device and there are new documentation requirements.
March 1, 2017Medical DevicesFDA
Hidrex GmbH recalls Hidrex USA DP450
Hazard: The device was reclassified from a class III device to a class II device and there are new documentation requirements.