FDA Recall Open, Classified

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

Recall: Z-0810-2025 · Initiated November 25, 2024

Recall

Recall Number
Z-0810-2025
Event Number
95910
Firm
Spacelabs Healthcare, Inc.
FEI Number
3010157426
Product Code
MHX
Status
Open, Classified
Root Cause
Software change control
Initiated
November 25, 2024
Posted
January 7, 2025
Address
35301 Se Center St, Snoqualmie, WA, 98065-9216

Description

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

Reason

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.

Action

On 11/25/2024, correction notices were emailed to customers who were asked to do the following: Firm will contact you at the earliest possible date to schedule a convenient time to update affected devices to software version 1.4.2 for XTR systems which addresses this defect. You can also contact GTS to have an FSE paged out for discussing upgrade schedule: 1-800-522-7025 and select 2 for Technical Support. Complete and submit the customer acknowledgement form: https://spacelabshealthcare.com/support/recall-reply-form/recall-reply-form-xtr-15-nov-2024/ For additional information or technical assistance, or to report an adverse event, contact: Technical Support: 1-800-522-7025 and select 2

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.

Quantity

434