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.
Other Recalls by Spacelabs Healthcare, Inc.
- Class II: Risk 09/05/2025
- Class II: Risk 09/05/2025
- Class II: Risk 09/05/2025
- Class II: Risk 11/25/2024
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.