Recall Z-1116-2017— Siemens Medical Solutions USA, Inc

Name: FDA recall Z-1116-2017
Creator: U.S. Food and Drug Administration
Published: 2017-01-11

Class II · Terminated

Class II FDA medical device recall by Siemens Medical Solutions USA, Inc, initiated 2017-01-11, terminated 2017-11-16. It names one FDA 510(k) clearance: K093612. Product: Syngo.plaza, picture archiving and communications system.. Reason: Software update for improvements and to resolve several issues.

Recalling firm: Siemens Medical Solutions USA, Inc
Classification: Class II
Status: Terminated
Initiated: 2017-01-11
Terminated: 2017-11-16
Firm location: Malvern, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K093612 — SYNGO.PLAZASiemens AG Medical Solutions·cleared 2010-03-04

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Syngo.plaza, picture archiving and communications system.

Reason for recall

Software update for improvements and to resolve several issues

Data sourced from openFDA. This site is unofficial and independent of the FDA.