FDAJanuary 30, 2017device
Daavlin Aquex (DAAV1000)
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
What to do
FDA enforcement status: Terminated
Brands named
hidrex
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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