Hidrex USA DVP1000 recall
Hidrex USA DVP1000
Why was Hidrex USA DVP1000 recalled?
The device was reclassified from a class III device to a class II device and there are new documentation requirements.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
SN# 16-3.6190 to 16-3.6319, 17-3.6001 to 17-3.6050
- Product
- Hidrex USA DVP1000
- Recalling firm
- Hidrex GmbH
- Quantity
- 180 units
- Distribution
- Nationwide throughout the US
- Recall date
- March 1, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)