Model Number 27918 |
Device Problems
Premature Discharge of Battery (1057); Battery Problem (2885)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/14/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The device was returned to resmed and an evaluation confirmed the complaint.The battery was replaced to address this issue.The device was serviced and fully tested before it was returned to the customer.(b)(4).
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Event Description
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It was reported to resmed that an astral device had a battery with a reduced level of capacity.There was no patient harm or serious injury reported as a result of this incident.
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Event Description
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It was reported to resmed that an astral device had a battery with a reduced level of capacity.There was no patient harm or serious injury reported as a result of this incident.
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Manufacturer Narrative
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The device was returned to resmed and an evaluation was performed.The reported complaint could not be confirmed.The battery was replaced as a precaution.The device was serviced and fully tested before it was returned to the customer.Resmed's risk analysis for this failure mode concludes that the risk is acceptable.Resmed reference#: (b)(4).
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Search Alerts/Recalls
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