Model Number 1185-3E080 |
Device Problems
Nonstandard Device (1420); Occlusion Within Device (1423); Product Quality Problem (1506); Manufacturing, Packaging or Shipping Problem (2975); No Flow (2991)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Patient Involvement (2645); No Known Impact Or Consequence To Patient (2692)
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Event Date 07/22/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Event took place in the us and has been reported through us distributor.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) reporter's narrative: needles are blocked.Sending 1 out of 5 for evaluation since 4 of the needles were discarded by physician prior to contacting pajunk.
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Manufacturer Narrative
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Based on risk assessment and clinical evaluation file is considered as closed.
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Event Description
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(b)(4).Reporter´s narrative: needles are blocked.Sending 1 out of 5 for evaluation since 4 of the needles were discarded by physician prior to contacting pajunk.
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Search Alerts/Recalls
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