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Hidrex GmbH recalls Daavlin Aquex (DAAV1000)
Recalled March 1, 2017 · FDA recall Z-1238-2017 · Hidrex
Hazard
The device was reclassified from a class III device to a class II device and there are new documentation requirements. · FDA Class III
Units
250 units
Sold at
Nationwide throughout the US
Description
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
Product
Daavlin Aquex (DAAV1000)
Manufacturer(s)
Hidrex GmbH
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →