Catalog Number 0940000000 |
Device Problems
Electrical /Electronic Property Problem (1198); Material Frayed (1262)
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Patient Problem
No Patient Involvement (2645)
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Event Date 05/27/2015 |
Event Type
malfunction
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Event Description
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It was reported that during inspection at the user facility the device cord was frayed, presenting an electric shock risk.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Event Description
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It was reported that during inspection at the user facility the device cord was frayed, presenting an electric shock risk.No patient involvement, no delay, no medical intervention and no adverse consequences were reported with this event.
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Manufacturer Narrative
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The device is available for evaluation but has not yet been received.Additional information will be submitted once the device is received and the quality investigation is completed.The device has not been returned for analysis at this time.
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Manufacturer Narrative
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The reported event was confirmed.Service evaluation found that the cord was damaged.The device was repaired and returned to the customer.
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Search Alerts/Recalls
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