PlainRecalls
FDA Devices Moderate Class II Terminated

Cios care fusion system

Reported: July 17, 2019 Initiated: June 20, 2019 #Z-1954-2019

Product Description

Cios care fusion system

Reason for Recall

DAP chamber may be missing an insulating foil

Details

Units Affected
1
Distribution
IL, NE
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
Cios care fusion system. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 1.
Why was this product recalled?
DAP chamber may be missing an insulating foil
Which agency issued this recall?
This recall was issued by the FDA Devices on July 17, 2019. Severity: Moderate. Recall number: Z-1954-2019.