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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K120616
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FDA Recall
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Spacelabs Healthcare qube Compact Patient Monitor, Model 91390. It is a patient monitor with arrhyt... 2 11/18/2013 Spacelabs Healthcare, Llc
Spacelabs Healthcare elance Vital Signs Monitor, Model 93300, with Option S. It is a patient monito... 2 11/08/2013 Spacelabs Healthcare, Llc
qube Compact Monitor (Patient Monitor) 91390. The monitor is 26.2 cm x 31.5 cm x 13.2 cm and weighs... 2 11/20/2012 Spacelabs Healthcare, Llc
Spacelabs qube Compact Monitor, Model 91390. The monitor is functioning as either bedside or centra... 2 05/13/2015 Spacelabs Healthcare Inc
Spacelabs Healthcare qube Compact Monitor, Model 91390. The Spacelabs Healthcare qube Compact M... 2 02/24/2015 Spacelabs Healthcare Inc
Spacelabs Healthcare Qube Compact Monitor, Model 91390. Intended to alert the user to alarm condi... 2 06/23/2014 Spacelabs Healthcare Inc
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