Spacelabs Healthcare Xhibit Central Station — Class II medical device recall Z-2885-2016
Terminated recall by Spacelabs Healthcare Inc, reported 2016-10-05, distributed nationwide. The firm received multiple reports of Xhibit Telemetry System going offline or locking up. In addition, short-
| Recall number | Z-2885-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spacelabs Healthcare Inc, Snoqualmie, WA, United States |
| Recall initiated | 2016-08-25 |
| Classified | 2016-09-26 |
| Reported by FDA | 2016-10-05 |
| Terminated | 2017-03-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, CN, DE, FR, GB, IE, IT, NL, PH, PL, RO |
| Model numbers | 96102 |
Product
Spacelabs Healthcare Xhibit Central Station, Model 96102, Version 1.1.2. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Reason for recall
The firm received multiple reports of Xhibit Telemetry System going offline or locking up. In addition, short-duration asystole alarms may not display an audio and visual alarm as reported from a single Canadian hospital.
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-2885-2016. 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.