Hidrex GmbH: Medical Device Recall in 2017 - (Recall #: Z-1236-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Hidrex USA DP450

Product Classification:

Class III

Date Initiated: January 30, 2017

Date Posted: March 1, 2017

Recall Number: Z-1236-2017

Event ID: 76362

Reason for Recall:

The device was reclassified from a class III device to a class II device and there are new documentation requirements.

Status: Terminated

Product Quantity: 64 units

Code Information:

SN# 16-3.7091 to 16-3.7134, 17-3.7001 to 17-3.7020

Distribution Pattern:

Nationwide throughout the US

Voluntary or Mandated:

Voluntary: Firm initiated