FDA recall Z-0810-2025

Spacelabs Healthcare, Inc. · Class II · device

Product

Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.

Reason for recall

Telemetry receivers with affected software versions may experience unsolicited system shut down and restart (Offline displayed), lasting approximately 1 to 1.5 minutes, which will cause temporary loss of monitoring. If a clinical event occurred during this period, staff may not detect until the system restarts and necessary clinical intervention could be delayed.

Distribution

US: MN, TX, TN, SC, OK, NM, GA, PA, OH, IA, AL, CO, AR, FL, MO, ME, LA, IL, WA, MA, WI, OR, MS, ID, NY, KS, PR. OUS: Canada, Taiwan, Czech Republic, France, Greece, Italy, Kuwait, Philippines, Poland.

Key facts

Status
Ongoing
Initiation date
2024-11-25
Report date
2025-01-15
Voluntary/Mandated
Voluntary: Firm initiated
Location
Snoqualmie, WA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0810-2025