PlainRecalls
FDA Devices Moderate Class II Terminated

Siemens Mobilette Mira, intended use as Mobile x-ray system.

Reported: December 12, 2012 Initiated: October 10, 2012 #Z-0480-2013

Product Description

Siemens Mobilette Mira, intended use as Mobile x-ray system.

Reason for Recall

There is a risk of lost images during examination.

Details

Units Affected
21
Distribution
Nationwide distribution: USA including states of: GA, ID, IL, IA, NE, NC, OH, SD, TX, and WI.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Siemens Mobilette Mira, intended use as Mobile x-ray system.. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 21.
Why was this product recalled?
There is a risk of lost images during examination.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 12, 2012. Severity: Moderate. Recall number: Z-0480-2013.