CLASS II Device recall · Reported 5 Oct 2016 · FDA Enforcement Report
Xhibit Telemetry Receiver (XTR) recalled by Spacelabs Healthcare
Spacelabs Healthcare is recalling Xhibit Telemetry Receiver (XTR), distributed nationwide in the US. The recall was initiated on 25 Aug 2016 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2886-2016
- FDA event ID
- 75078
- Recalling firm
- Spacelabs Healthcare, Snoqualmie, WA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 25 Aug 2016
- FDA classified
- 26 Sep 2016
- Reported
- 5 Oct 2016
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Patient Monitors
Timeline
| 25 Aug 2016 | Recall initiated by company | |
| 26 Sep 2016 | Classified by FDA | +32 days |
| 5 Oct 2016 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
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.
Where it was distributed
Worldwide distribution. US nationwide including Puerto Rico, Australia, Canada, China, France, Germany, Ireland, Italy, Netherlands, Philippines, Poland, Romania, Switzerland, and United Kingdom.
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
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.
Where was it sold?
Worldwide distribution. US nationwide including Puerto Rico, Australia, Canada, China, France, Germany, Ireland, Italy, Netherlands, Philippines, Poland, Romania, Switzerland, and United Kingdom.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 75078| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Xhibit Central Station recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | Nationwide |
More recalls from Spacelabs Healthcare
All 47| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Xhibit Central Station recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Spacelabs Ultraview SL Command Module SL Command Module recalled | Spacelabs Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Multi-parameter Command Module recalled by Spacelabs Healthcare | Spacelabs Healthcare | Labeling Errors | Nationwide |
| Device | CLASS II | Sentinel V11 recalled by Spacelabs Healthcare | Spacelabs Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Branding is not applied to this product DVI display cables recalled | Spacelabs Healthcare | Device Malfunction | Nationwide |
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| Device | CLASS I | Bravo CF capsule delivery device, Product Number FGS recalled | Given Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Lux-Dx, Lux-Dx II, Lux-Dx II+ Insertable Cardiac Monitor recalled | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | IQecg Digital ECG recalled by Midmark | Midmark | Labeling Errors | Nationwide |