The Spacelabs Healthcare Xhibit Telemetry Receiver — Class II medical device recall Z-1502-2016
Terminated recall by Spacelabs Healthcare Inc, reported 2016-04-27, distributed in AL, AZ, CA, CO, CT, FL, ID, IN…. Reports of an abnormally high frequency of squelch events on Xhibit Telemetry Receivers (XTR), which is indica
| Recall number | Z-1502-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spacelabs Healthcare Inc, Snoqualmie, WA, United States |
| Recall initiated | 2016-03-28 |
| Classified | 2016-04-15 |
| Reported by FDA | 2016-04-27 |
| Terminated | 2016-12-19 |
| Distributed | AL, AZ, CA, CO, CT, FL, ID, IN, KY, MI, MN, MO, MS, MT, SC, TX, WY |
| Countries outside the US | AU, CA, CN, FR, GB, NL, PH, RO |
| Model numbers | 040-1736-00KIT, 96280 |
Product
The Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280 is used to transmit patient(s) physiological measurements and data to a monitor.
Reason for recall
Reports of an abnormally high frequency of squelch events on Xhibit Telemetry Receivers (XTR), which is indicative of the loss of the telemetry data signal. In some cases, the Xhibit Central Monitor was also reported to display an Xhibit Offline error message for all patients being monitored.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1502-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.