Spacelabs Healthcare, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0809-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 25, 2024

Date Posted: January 15, 2025

Recall Number: Z-0809-2025

Event ID: 95927

Reason for Recall:

Telemetry receiver systems may experience a Windows proxy Issue causing the system to 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; necessary clinical intervention could be delayed.

Status: Ongoing

Product Quantity: 2265

Code Information:

Service Manuals P/N 070-2409-07 and Prior. UDI-DI: 10841522107177, 10841522100246

Distribution Pattern:

US: OK, MN, IA, SC, NE, MI, NY, KY, GA, MO, MT, LA, WA, SD, CO, PA, WY, TX, ID, NJ, FL, OH, MS, OR, AK, IL, AR, KS, AL, TN, WI, VA, NM, CA, IN, RI, NV, MA, NC, ME, CT, AZ, MD, PR. OUS: Kuwait, Australia, Canada, Roumanie, Greece, Philippines, Spain, Italy, Hong Kong, Switzerland, Panama, Taiwan, Netherlands, Malaysia, Poland, Mexico, United Kingdom, Saudi Arabia, France, Czech Republic

Voluntary or Mandated:

Voluntary: Firm initiated