FDAMay 31, 2022device

Xhibit Telemetry Receiver, Model: 96280

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure.

What to do

FDA enforcement status: Ongoing

Brands named

spacelabs healthcarespacelabs

UPCs

10841522100246

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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