PlainRecalls
FDA Devices Moderate Class II Terminated

ONCOR" Avant-garde

Reported: March 29, 2017 Initiated: February 14, 2017 #Z-1490-2017

Product Description

ONCOR" Avant-garde

Reason for Recall

Software update

Details

Units Affected
80 systems
Distribution
Distributed throughout the United States
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
ONCOR" Avant-garde. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 80 systems.
Why was this product recalled?
Software update
Which agency issued this recall?
This recall was issued by the FDA Devices on March 29, 2017. Severity: Moderate. Recall number: Z-1490-2017.