Spacelabs Healthcare, Inc.: Device Recall

Recall #Z-0810-2025 · 11/25/2024

Class II: Risk

Recall Details

Recall Number
Z-0810-2025
Classification
Class II
Product Type
Device
Recalling Firm
Spacelabs Healthcare, Inc.
Status
Ongoing
Date Initiated
11/25/2024
Location
Snoqualmie, WA, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
434

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.

Product Description

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

Distribution Pattern

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.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.