Xhibit Central Station — Class II medical device recall Z-0332-2017
Terminated recall by Spacelabs Healthcare Inc, reported 2016-11-09, distributed in AL, CA, CT, FL, GA, IA, ID, IL…. The firm received reports of telemetry SpO2 numerics dropping off the Xhibit Central display. Desaturation, hi
| Recall number | Z-0332-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spacelabs Healthcare Inc, Snoqualmie, WA, United States |
| Recall initiated | 2016-10-18 |
| Classified | 2016-11-02 |
| Reported by FDA | 2016-11-09 |
| Terminated | 2017-04-03 |
| Distributed | AL, CA, CT, FL, GA, IA, ID, IL, IN, KY, MI, MN, MS, NC, NE, NJ, NY, OH, OK, PA, PR, RI, SC, SD, TX, VA, WA, WY |
| Countries outside the US | AU, CA, CH, CL, CZ, FR, GB, MX, NL, PA, SA, TW |
| Model numbers | 96102 |
Product
Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric and neonatal patient data of patients connected to networked Spacelabs Healthcare patient monitors and telemetry transmitters.
Reason for recall
The firm received reports of telemetry SpO2 numerics dropping off the Xhibit Central display. Desaturation, high, and low limit alarms work normally.
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-0332-2017. 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.