ARIATELE TELEMETRY TRANSMITTER — Class II medical device recall Z-0871-2014
Terminated recall by Spacelabs Healthcare, Llc, reported 2014-02-05, distributed nationwide. The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because the AriaTele (transmitter) display
| Recall number | Z-0871-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Spacelabs Healthcare, Llc, Snoqualmie, WA, United States |
| Recall initiated | 2013-12-19 |
| Classified | 2014-01-30 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2014-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CL, PA |
| Serial numbers | 002002, 002003, 002004, 002005, 002006, 002007, 002008, 002009, 002010, 002011, 002012, 002013, 6281, 6281-000295, 6281-000401, 6281-000402, 6281-000403, 6281-000404, 6281-000405, 6281-000406, 6281-000407, 6281-000408, 6281-000503, 6281-000504, 6281-000505 and 475 more |
| Model numbers | 96281 |
Product
ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or neonatal patient populations in a hospital environment.
Reason for recall
The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because the AriaTele (transmitter) display and the Telemetry Central Station display may show a SpO2 value when the sensor is not connected to the patient or in certain sensor failed conditions.
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-0871-2014. 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.