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Model Number N/A |
Device Problem
Insufficient Information (3190)
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Patient Problems
Inflammation (1932); Loss of Range of Motion (2032); Weakness (2145)
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Event Type
Injury
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Manufacturer Narrative
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Current information is insufficient to permit conclusions as to the cause of the events.Event details and product identification were not provided for the patient mentioned in the journal article.The following sections could not be completed with the limited information provided.B3 ¿ date of event ¿ ni.D2 ¿ device product code ¿ ni.D4 ¿ expiration date ¿ ni.D6 ¿ date implanted ¿ ni.D7 ¿ date explanted ¿ ni.E1 -- initial reporter - the article was written by: culp, randall w.; bachoura, abdo; gelman, scott e.; and jacoby, sidney m.H4 ¿ manufacture date ¿ ni.
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Event Description
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Information was received based on review of a journal article titled, " proximal row carpectomy combined with wrist hemiarthroplasty " which aimed to present early experience with proximal row carpectomy (prc) combined with distal radius hemiarthroplasty using the maestro wrist reconstructive system radial component, manufactured by legacy biomet from april 2009 to june 2010.A competitor product was used from september 2010 onwards.17 patients were identified in the article that underwent proximal row carpectomy combined with distal radius hemiarthroplasty with a maestro radial component on an unknown date.Mean postoperative flexion, extension, and grip strength were all less than preoperative levels.It was reported that a (b)(6) with a history of slac iii wrist and posttraumatic arthritis underwent left wrist arthroplasty.Patient subsequently experienced flexor tenosynovitis and underwent flexor tenosynovectomy.No further information is available.
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Search Alerts/Recalls
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