FDA recall Z-1513-2022

Spacelabs Healthcare, Inc. · Class II · device

Product

Xhibit Telemetry Receiver, Model: 96280

Reason for recall

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.

Distribution

Worldwide distribution - US Nationwide distribution in the states of NY, AR, CO, FL, NJ, AL, KY, TN, SC, WA, OK, MN, PA, GA, VA, CA, OH, IA, KS, MI, IN, TX, MT, MO, ME, LA, IL, SD, MA, OR, ID, MD, AZ, AK and the countries of MB, ON, FR, QC, BC, IS, CT, RM.

Key facts

Status
Ongoing
Initiation date
2022-05-31
Report date
2022-08-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Snoqualmie, WA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1513-2022