Ziehm Imaging Inc: Medical Device Recall in 2014 - (Recall #: Z-0566-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging

Product Classification:

Class II

Date Initiated: November 21, 2013

Date Posted: January 1, 2014

Recall Number: Z-0566-2014

Event ID: 66976

Reason for Recall:

Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.

Status: Terminated

Product Quantity: 1 device

Code Information:

90842

Distribution Pattern:

USA (Nationwide) Distribution including the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MT, MA, MD, MI, MN, MN, MO,MS, NC ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Hawaii.

Voluntary or Mandated:

Voluntary: Firm initiated