It was reported that the patient underwent a right knee arthroplasty revision to address post-operative instability and requiring a different length to stabilize the leg once again approximately six (6) months post-operatively.Attempts have been made, however, no additional information is available.
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(b)(4).D10 - concomitant devices - orthopaedic salvage system poly locking pin, catalog #: 150478, lot #: 816710; orthopaedic salvage system elliptical diaphyseal segment 3cm, catalog #: 150461, lot #: 230920; orthopaedic salvage system segmental femoral component 7cm right ,catalog # 150354, lot #: 782310; orthopaedic salvage system modular tibial baseplate 79mm, catalog #: 150424, lot #: 689560; series a thin 3-peg patella 37mm x 8.6mm, catalog #: 184788, lot #: 277320; orthopaedic salvage system tibial poly bearing 16mm, catalog #: 150412, lot #: 622440; orthopaedic salvage system reinforced yoke, catalog #: 150493, lot #: 293580; orthopaedic salvage system poly femoral bushings 2pk, catalog #: 150477, lot #: 096430; orthopaedic salvage system axle, catalog #: 150480, lot #: 942420; orthopaedic salvage system poly tibial bushing, catalog #: 150476, lot #: 540910.The complainant has indicated that the product will not be returned to zimmer biomet for investigation, as the devices were discarded.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this patient; please see all reports associated with this event: 0001825034-2023-01927, 0001825034-2023-01928, 0001825034-2023-01929.H3 other text: investigation incomplete.
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