Hidrex Recalls Daavlin Aquex Devices Due to Documentation Requirements
Hidrex GmbH is recalling 250 Daavlin Aquex (DAAV1000) devices nationwide because the device was reclassified from Class III to Class II, triggering new documentation requirements.
- Product
- Daavlin Aquex (DAAV1000)
- Category
- Medical Device
- Distribution
- Distributed nationwide