Catalog Number ASK-45703-VAMCP |
Device Problems
Device Damaged Prior to Use (2284); Device Markings/Labelling Problem (2911)
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Patient Problem
No Patient Involvement (2645)
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Event Date 03/11/2020 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).
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Event Description
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The customer reports that when they opened a kit they realized it was a single lumen and not a three lumen catheter.
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Manufacturer Narrative
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Qn#(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.A device history record review was performed and no relevant findings were identified.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.If the sample becomes available at a later date a follow up report will be submitted with investigation results.
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Event Description
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The customer reports that when they opened a kit they realized it was a single lumen and not a three lumen catheter.
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Search Alerts/Recalls
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