Model Number 0331152-51 |
Device Problems
Mechanical Problem (1384); Device Operates Differently Than Expected (2913); Device Handling Problem (3265)
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Patient Problems
Awareness during Anaesthesia (1707); No Code Available (3191)
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Event Date 01/04/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Event took place in (b)(6).At this time neither detailed information nor the device is available.As soon as more data is accessible a follow up report will be sent in.Not yet returned.
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Event Description
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(b)(4).The sealing inside the lor-syringe got loosened; unable to identify epidural space via lor-technique.
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Manufacturer Narrative
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Event took place in (b)(6).If no further information becomes available, this particular file is considered as closed.
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Event Description
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(b)(4).The sealing inside the lor-syringe got loosened; unable to identify epidural space via lor-technique.
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Search Alerts/Recalls
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