Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (X...
FDA Device Recall #Z-2886-2016 — Class II — August 25, 2016
Recall Summary
| Recall Number | Z-2886-2016 |
| Classification | Class II — Moderate risk |
| Date Initiated | August 25, 2016 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Spacelabs Healthcare Inc |
| Location | Snoqualmie, WA |
| Product Type | Devices |
| Quantity | 316 XTR units total (248 units in the US and 68 units outside US) |
Product Description
Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Reason for Recall
The firm received multiple reports of Xhibit Telemetry System going offline or locking up. In addition, short-duration asystole alarms may not display an audio and visual alarm as reported from a single Canadian hospital.
Distribution Pattern
Worldwide distribution. US nationwide including Puerto Rico, Australia, Canada, China, France, Germany, Ireland, Italy, Netherlands, Philippines, Poland, Romania, Switzerland, and United Kingdom.
Lot / Code Information
Serial numbers of units distributed in the US 6280-000053, 6280-000056, 6280-000057, 6280-000058, 6280-000059, 6280-000066, 6280-000067, 6280-000068, 6280-000077, 6280-000078, 6280-000079, 6280-000083, 6280-000084, 6280-000085, 6280-000086, 6280-000088, 6280-000090, 6280-000092, 6280-000093, 6280-000095, 6280-000096, 6280-000097, 6280-000098, 6280-000099, 6280-000100, 6280-000101, 6280-000102, 6280-000103, 6280-000104, 6280-000105, 6280-000106, 6280-000107, 6280-000108, 6280-000109, 6280-000110, 6280-000111, 6280-000112, 6280-000113, 6280-000114, 6280-000115, 6280-000116, 6280-000117, 6280-000118, 6280-000120, 6280-000121, 6280-000122, 6280-000123, 6280-000124, 6280-000125, 6280-000126, 6280-000127, 6280-000128, 6280-000129, 6280-000131, 6280-000132, 6280-000137, 6280-000138, 6280-000140, 6280-000141, 6280-000142, 6280-000143, 6280-000146, 6280-000147, 6280-000148, 6280-000149, 6280-000151, 6280-000152, 6280-000153, 6280-000154, 6280-000155, 6280-000156, 6280-000158, 6280-000159, 6280-000160, 6280-000161, 6280-000167, 6280-000168, 6280-000170, 6280-000171, 6280-000172, 6280-000173, 6280-000174, 6280-000176, 6280-000177, 6280-000200, 6280-000228, 6280-000229, 6280-000233, 6280-000234, 6280-000235, 6280-000236, 6280-000238, 6280-000239, 6280-000240, 6280-000241, 6280-000242, 6280-000243, 6280-000245, 6280-000250, 6280-000251, 6280-000252, 6280-000253, 6280-000254, 6280-000255, 6280-000256, 6280-000257, 6280-000260, 6280-000261, 6280-000263, 6280-000264, 6280-000265, 6280-000266, 6280-000267, 6280-000268, 6280-000269, 6280-000271, 6280-000272, 6280-000273, 6280-000274, 6280-000275, 6280-000278, 6280-000279, 6280-000280, 6280-000281, 6280-000283, 6280-000284, 6280-000285, 6280-000286, 6280-000287, 6280-000288, 6280-000289, 6280-000298, 6280-000301, 6280-000302, 6280-000303, 6280-000306, 6280-000307, 6280-000308, 6280-000310, 6280-000311, 6280-000312, 6280-000315, 6280-000316, 6280-000318, 6280-000319, 6280-000321, 6280-000322, 6280-000324, 6280-000326, 6280-000327, 6280-000328, 6280-000329, 6280-000332, 6280-000333, 6280-000334, 6280-000338, 6280-000341, 6280-000342, 6280-000343, 6280-000344, 6280-000345, 6280-000346, 6280-000347, 6280-000348, 6280-000349, 6280-000350, 6280-000351, 6280-000352, 6280-000353, 6280-000354, 6280-000355, 6280-000357, 6280-000358, 6280-000363, 6280-000364, 6280-000365, 6280-000366, 6280-000367, 6280-000368, 6280-000369, 6280-000370, 6280-000375, 6280-000376, 6280-000377, 6280-000378, 6280-000380, 6280-000381, 6280-000382, 6280-000383, 6280-000385, 6280-000386, 6280-000387, 6280-000388, 6280-000389, 6280-000390, 6280-000391, 6280-000392, 6280-000394, 6280-000395, 6280-000396, 6280-000397, 6280-000398, 6280-000399, 6280-000402, 6280-000403, 6280-000404, 6280-000407, 6280-000408, 6280-000409, 6280-000410, 6280-000411, 6280-000412, 6280-000413, 6280-000414, 6280-000415, 6280-000417, 6280-000418, 6280-000419, 6280-000420, 6280-000421, 6280-000423, 6280-000426, 6280-000427, 6280-000429, 6280-000430, 6280-000431, 6280-000432, 6280-000436, 6280-000437, 6280-000438, 6280-000439, 6280-000440, 6280-000455, 6280-000456, 6280-000457, 6280-000458, 6280-000459, 6280-000460, 6280-000461, 6280-000462, 6280-000463, 6280-000464, 6280-000465, 6280-000466, 6280-000467, 6280-000468, 6280-000475, 6280-000476. Serial numbers of units distributed OUTSIDE the US 6280-000048, 6280-000050, 6280-000052, 6280-000060, 6280-000061, 6280-000062, 6280-000063, 6280-000064, 6280-000065, 6280-000076, 6280-000094, 6280-000178, 6280-000179, 6280-000181, 6280-000182, 6280-000183, 6280-000184, 6280-000185, 6280-000186, 6280-000188, 6280-000190, 6280-000191, 6280-000193, 6280-000194, 6280-000195, 6280-000196, 6280-000197, 6280-000198, 6280-000199, 6280-000202, 6280-000225, 6280-000226, 6280-000231, 6280-000232, 6280-000237, 6280-000246, 6280-000247, 6280-000249, 6280-000262, 6280-000270, 6280-000276, 6280-000282, 6280-000290, 6280-000291, 6280-000292, 6280-000293, 6280-000294, 6280-000295, 6280-000297, 6280-000300, 6280-000305, 6280-000317, 6280-000330, 6280-000331, 6280-000356, 6280-000362, 6280-000371, 6280-000372, 6280-000384, 6280-000400, 6280-000401, 6280-000406, 6280-000416, 6280-000424, 6280-000425, 6280-000433, 6280-000435, and 6280-000473.
Other Recalls from Spacelabs Healthcare Inc
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-0532-2018 | Class II | Spacelabs Healthcare Xhibit Telemetry Receiver,... | Jan 17, 2018 |
| Z-0332-2017 | Class II | Xhibit Central Station, Model 96102. Inten... | Oct 18, 2016 |
| Z-2885-2016 | Class II | Spacelabs Healthcare Xhibit Central Station, Mo... | Aug 25, 2016 |
| Z-2343-2016 | Class II | 91496 Ultraview SL Command Module, Options A, B... | Jul 1, 2016 |
| Z-1502-2016 | Class II | The Spacelabs Healthcare Xhibit Telemetry Recei... | Mar 28, 2016 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.