FDA recall record

Spacelabs Healthcare ARIATELE TELEMETRY TRANSMITTER, Model 96281, with SpO2 Option C recall — FDA Z-0871-2014

The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because the AriaTele (transmitter) display and the Telemetry Central Station display…

Class IIclassification
Z-0871-2014official record ID
Feb 5, 2014report date

Recall record at a glance

Official recordZ-0871-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSpacelabs Healthcare, LLC
Report dateFeb 5, 2014
Recall initiation dateDec 19, 2013
Quantity1057 units (988 in the US and 69 outside of the US).
LocationSnoqualmie, WA, United States

Official product description

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.

Why the product was recalled

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.

Distribution information

Worldwide Distribution: US (nationwide) including states of: AZ, CA, FL, GA, IA, IL, LA, MA, ME, MI, MO, MS, NY, PA, SC, TN, TX, VA, and Puerto Rico; and Internationally to: Canada, Chile, and Panama.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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