PlainRecalls
FDA Devices Moderate Class II Terminated

Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems

Reported: April 19, 2017 Initiated: October 17, 2016 #Z-1770-2017

Product Description

Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems

Reason for Recall

Due to a potential manufacturing error, a rare possibility exists for a sudden drop in table height of the Combi Dockable Table Neurosurgery.

Details

Units Affected
3 systems distributed in the U.S.
Distribution
US Distribution to: DC and MD.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 3 systems distributed in the U.S..
Why was this product recalled?
Due to a potential manufacturing error, a rare possibility exists for a sudden drop in table height of the Combi Dockable Table Neurosurgery.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 19, 2017. Severity: Moderate. Recall number: Z-1770-2017.