The following sections could not be completed with the limited information provided: date of birth-ni.Weight-ni.Udi - (b)(4).Concomitant medical products: item141314, biomet finned pri stem 40 mm with screw, lot 082960.Item184768, vanguard series a standard patella, lot 772770.Item ep-183460, vanguard cr tibial bearing, lot 571090.Item 183012, vanguard (tm) cr interlok femoral-rt, lot 909410.This report is number 2 of 5 mdrs filed for the same patient (reference 0001825034-2017-00409/0001825034-2017-0040/0001825034-2017-00411/0001825034-2017-00410/0001825034-2017-00412).
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This follow-up report is being filed to relay additional information, which was unknown at the time of the initial medwatch.The review of device history records discovered no deviations or abnormalities that are related to this event.The following components were reviewed for compatibility with no issues noted.These devices are used for treatment.Root cause could not be determined with information available.No corrective actions, preventive actions, or field actions resulted after investigation of this event.
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