Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was reclassified from a class III...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hidrex GmbH directly.
Affected Products
Hidrex USA DVP1000
Quantity: 180 units
Why Was This Recalled?
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hidrex GmbH
Hidrex GmbH has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report