Xhibit Telemetry Receiver with Software, Model 96280. Intended to provide monitoring system with patient data.
FDA device recall Z-0810-2025 · posted 2025-01-07 · Open, Classified
Recall details
- Recalling firm
- Spacelabs Healthcare, Inc.
- 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.
- Action taken
- 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
- Root cause
- Software change control
- Status
- Open, Classified
- Product code
- MHX
- Quantity affected
- 434
- 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.
- Date initiated
- 2024-11-25
- Date posted
- 2025-01-07
- Location
- Snoqualmie, WA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SPACELABS HEALTHCARE TELEMETRY RECEIVER (K141156) | Spacelabs Healthcare | 2014-09-09 |