Recall Z-1514-2015— Sony Latin America

Class II · Terminated

Class II FDA medical device recall by Sony Latin America, initiated 2015-03-05, terminated 2016-12-14. FDA's recall record names no specific 510(k) clearance for this event. Product: Sony Medical Monitor LMD-1951MD 19 inch. Reason: Monitor has either not turned on or has lost image during clinical use..

Recalling firm
Sony Latin America
Classification
Class II
Status
Terminated
Initiated
2015-03-05
Terminated
2016-12-14
Firm location
Miami, FL, United States

Product description

Sony Medical Monitor LMD-1951MD 19 inch

Reason for recall

Monitor has either not turned on or has lost image during clinical use.

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