FDAClass IIApril 19, 2017

Combi Dockable Neurosurgery table for the Siemens recall

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

Why was Combi Dockable Neurosurgery table for the Siemens recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Model Number: 10684336, 10684337 Serial Number: 12811002 12811003 12811017

Product
Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems
Recalling firm
Siemens Medical Solutions USA, Inc
Quantity
3 systems distributed in the U.S.
Distribution
US Distribution to: DC and MD.
Recall date
April 19, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls