All product features corresponded with the valid specifications of the waldemar link (b)(4) at the time, when the item was produced.The batch documentation review incl.The quality inspection reports did not reveal irregularities or deviations in the production process.The implant corresponds with our specifications.The visual inspection shows the uhmwpe bushing is worn.It is assumed that functional overload due to poor soft tissue constitution is the cause for damaged and worn rotational bushing.Obesity with a bmi of 35,3 contributed to the wear of the bushing.The waldemar link (b)(4) is aiming for the highest product quality and trying to keep the failure rate as low as possible by means of the customer feedback.Permanent employee trainings and market surveillance are performed.The report is delayed due to inconsistencies with regard to foreign event reporting to fda.After re-evaluation of the complaint we determined that it is reportable.We have addressed the inconsistency in reporting foreign events to fda through capa-(b)(4).
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