Xhibit Telemetry Receiver, Model: 96280
Check against the official notice below — it lists the full affected range.
Spacelabs Healthcare is recalling 529 units of its Xhibit Telemetry Receiver, Model 96280, with software version 1.4.0 due to a software defect that occurs after approximately 25 days of continuous use. The defect prevents proper alarm escalation for critical technical alarms including signal loss, all leads off, low battery, SpO2 sensor off, and signal interference. Because alarm escalation does not function as intended, caregivers may not respond to the initial technical alarm and may remain unaware that a continuing technical failure is occurring.
The affected devices have been distributed nationwide across numerous U.S. states and in Canadian provinces and other international locations. The recall identifies specific serial numbers and applies to UDI-DI 10841522100246 with software version 1.4.0. The source does not specify what remedy consumers should take.
Written by software from the official notice below. Not reviewed by a lawyer.
Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure.
Reason for recall: Software related alarm escalation defect occurs after approximately 25 days of continuous use. Technical alarm escalation for the following alarms, signal loss, all leads off, low battery, SpO2 sensor off, and signal interference, does not occur in the telemetry receiver as specified. Caregiver may not respond to the initial technical alarm and may not be aware of the continuing technical failure. Distribution: Worldwide distribution - US Nationwide distribution in the states of NY, AR, CO, FL, NJ, AL, KY, TN, SC, WA, OK, MN, PA, GA, VA, CA, OH, IA, KS, MI, IN, TX, MT, MO, ME, LA, IL, SD, MA, OR, ID, MD, AZ, AK and the countries of MB, ON, FR, QC, BC, IS, CT, RM. Quantity: 529 Lot/code info: UDI-DI: 10841522100246, Software version 1.4.0. Serial Numbers: 6280-001538, 6280-000590, 6280-000589, 6280-000339, 9280-000711, 6280-001103, 6280-001102, 6280-001469, 6280-001467, 6280-001686, 6280-001399, 6280-001323, 6280-000457, 6280-000456, 6280-000455, 6280-000440, 6280-000439, 6280-000438, 6280-000429, 6280-000476, 6280-000475, 6280-001693, 6280-000703, 6280-000702, 6280-000701, 6280-000700, 6280-000314, 6280-000258, 6280-000157, 6280-001223, 6280-001222, 6280-001221, 6280-001220, 6280-001219, 6280-001218, 6280-001217, 6280-001216, 6280-001215, 6280-001214, 6280-001207, 6280-001127, 6280-001125, 6280-001124, 6280-001123, 6280-001056, 6280-001055, 6280-001054, 6280-001053, 6280-001052, 6280-001051, 6280-001050, 6280-001288, 6280-001287, 6280-001490, 6280-001692, 6280-000588, 6280-000517, 6280-000516, 6280-000515, 6280-001668, 6280-000206, 6280-000162, 6280-000210, 6280-000663, 6280-000377, 6280-001589, 6280-001385, 6280-001384, 6280-001382, 6280-001405, 6280-000594, 6280-000593, 6280-000592, 6280-000596, 6280-000274, 6280-001844, 6280-001843, 6280-001721, 6280-001720, 6280-000136, 6280-001784, 6280-001783, 6280-000359, 6280-000340, 6280-000336, 6280-001718, 6280-001706, 6280-001705, 6280-001704, 6280-001703, 6280-001702, 6280-001699, 6280-001698, 6280-001672, 6280-001669, 6280-000622, 6280-001797, 6280-000097, 6280-001558, 6280-001551, 6280-001649, 6280-001648, 6280-001647, 6280-001646, 6280-001645, 6280-001594, 6280-000093, 6280-001168, 6280-001531, 6280-001670, 6280-0
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.