Model Number 021159-20D |
Device Problems
Patient-Device Incompatibility (2682); Device-Device Incompatibility (2919); Device Handling Problem (3265)
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Patient Problems
Pain (1994); Inadequate Pain Relief (2388)
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Event Date 10/07/2016 |
Event Type
Injury
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Manufacturer Narrative
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Event took place in (b)(6) and has been reported through (b)(4) distributor (b)(4).Currently the data is poor and the device has not been sent back/ analysed.As soon as further data will be available a follow up report will be sent in to the agency.
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Event Description
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(b)(4).Summarizing tentative translation from initial reporter's narrative: upon removal of the stylet the catheter curled up, catheter system had to be removed.
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Manufacturer Narrative
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Event took place in (b)(6) and has been reported through (b)(6).Based on risk assessment and clinical evaluation, file is considered as closed.
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Event Description
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(b)(4).Summarizing tentative translation from initial reporter´s narrative: upon removal of the stylet, the catheter curled up, catheter system had to be removed.
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Search Alerts/Recalls
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