(b)(4).The customer report of a foreign material observed was confirmed by investigation of the returned sample.The customer supplied photos and video confirmed that there were foreign particulates coming from inside the arrow raulerson syringe (ars) valve.The customer returned an opened cvc kit including an introducer needle, guide wire assembly, and arrow raulerson syringe (ars) for evaluation.Visual inspection revealed that there were no signs of use observed.Foreign material was observed within the ars handle and the guide wire assembly.Further analysis revealed that there was a hole in the internal valve of the ars.Microscopic examination confirmed the foreign material inside the ars handle and on the guide wire assembly.Further analysis revealed that there was not a noticeable hole or other signs of damage within the internal valve of the ars.As per r & d engineering and manufacturing unit, a positive confirmation of the material could not be made based on the appearance of the substance and the small quantity present within the straightener tube and ars handle.Additionally, it could not be confirmed when the particulate was introduced into the kit.A device history record review was performed, and no relevant findings were identified.Based on the appearance of the substance and the small quantity present within the components, a positive confirmation of the material could not be made.Additionally, it cannot be confirmed when the particulate was introduced into the kit.Based on the sample received, comments from r & d, and the complaint investigation, the potential root cause cannot be determined.Teleflex will continue to monitor and trend for complaints of this nature.
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