Ziehm Imaging Inc: Medical Device Recall in 2017 - (Recall #: Z-1893-2017)

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:

Ziehm Imaging solo FD Mobile Fluoroscopic C-arm

Product Classification:

Class II

Date Initiated: February 23, 2017

Date Posted: May 24, 2017

Recall Number: Z-1893-2017

Event ID: 77030

Reason for Recall:

During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component

Status: Terminated

Product Quantity: US - 2 systems

Code Information:

S/N 52199, 52108

Distribution Pattern:

US Distribution to the states of : FL and CA. No devices listed in this recall where distributed any foreign /military/government consignees from the U.S.A.

Voluntary or Mandated:

FDA Mandated