medical Class II Updated 2020-06-10

Spacelabs Healthcare, Inc. recalls Xhibit Central, Model No. 96102 - Product Usage: intended us

Recalled Product

Xhibit Central, Model No. 96102 - Product Usage: intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.


Hazard / Issue

The firm received reports of loss of audio alarm after a power failure or cable disconnection. The loss of audio for a telemetry patient could delay the recognition of an alarm condition.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model No. 96102 Xhibit Central; Software Versions: 1.3.1, 1.3.2, 1.3.3 and 1.3.4; UDI: 10841522100345
View official government recall

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