FDA Device recall Z-0871-2014
ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or neonatal patient popu…
- FDA Device
- Class II
- terminated
- Published 2014-02-05
On 2014-02-05 the FDA classified a Class II recall of ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C. Model 96281 is intended for use with either adult or neonatal patient popu… by Spacelabs Healthcare, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0871-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-19 |
| Published | 2014-02-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spacelabs Healthcare |
| Distribution | US |
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
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.
Identifiers
| code_info | Serial Numbers IN the US: 6281- 002002, 6281- 002003, 6281- 002004, 6281- 002005, 6281- 002006, 6281- 002007, 6281-…Serial Numbers IN the US: 6281- 002002, 6281- 002003, 6281- 002004, 6281- 002005, 6281- 002006, 6281- 002007, 6281- 002008, 6281- 002009, 6281- 002010, 6281- 002011, 6281- 002012, 6281- 002013, 6281-000295, 6281-000401, 6281-000402, 6281-000403, 6281-000404, 6281-000405, 6281-000406, 6281-000407, 6281-000408, 6281-000503, 6281-000504, 6281-000505, 6281-000506, 6281-000507, 6281-000508, 6281-000512, 6281-000513, 6281-000514, 6281-000515, 6281-000516, 6281-000517, 6281-000518, 6281-000519, 6281-000520, 6281-000521, 6281-000522, 6281-000523, 6281-000524, 6281-000526, 6281-000527, 6281-000528, 6281-000529, 6281-000530, 6281-000531, 6281-000532, 6281-000533, 6281-000534, 6281-000535, 6281-000536, 6281-000537, 6281-000538, 6281-000539, 6281-000540, 6281-000541, 6281-000542, 6281-000543, 6281-000544, 6281-000545, 6281-000546, 6281-000547, 6281-000549, 6281-000550, 6281-000551, 6281-000552, 6281-000553, 6281-000554, 6281-000555, 6281- |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Device · Class II · 2025-11-12 · Spacelabs Healthcare - Brand Name: Branding is not applied to this product
FDA Device · Class II · 2025-10-22 · Spacelabs Healthcare
All Spacelabs Healthcare recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0871-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.