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Class 2 Device Recall EasyFuse - Food and Drug …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=192433
    Wright Medical Technology, Inc. 1023 Cherry Rd Memphis TN 38117-5423: For Additional Information Contact: Meghan Wells 901-201-9298 Manufacturer Reason for Recall: The drill and adjustable drill guide can jam/bind intraoperatively resulting in the …

Medical Device Recalls

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&event_id=84180
    Related Medical Device Recalls 1 2 > Results per Page New Search ... Wright Medical Technology, Inc. Z-0563-2020 - ORTHOLOC 3DI PLT SYS STERILE, LOCKING …

Class 1 Device Recall PROFEMUR PLUS CoCr …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=139368
    2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see …

Wright Medical Hip Lawsuit – Verdicts & Settlements

    https://www.drugwatch.com/hip-replacement/wright-medical/lawsuits/
    The recall notice warned that an acute fracture of the device would require emergency surgery. It also warned that such a fracture in a Profemur hip stem could “lead to …

Guide to Wright Hip Replacement Recall …

    https://www.sidgilreath.com/learn/wright-hip-recall-lawsuit.html
    The Wright lawsuit settlements cover patients that experienced a substantial defect between 150 days and eight years after their surgery. The Wright implant devices …

Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
    Summaries of information about the most serious medical device recalls. These products are on the list because there is a reasonable chance that they could …

Class 2 Device Recall CONSERVE, TOTAL ACLASS …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=82544
    Wright Medical Technology, Inc. notified hospitals, surgeons and their distributors of the recall situation via an "Urgent: Medical Device Voluntary Recall" …

Wright Medical Group N.V. | a global …

    https://www.wright.com/
    Wright Medical Group N.V. is a global medical device company focused on Extremities and Biologics. We are a recognized leader of surgical solutions for the upper …

Wright Medical Technology, Inc. Recall 90216 – Product Safety …

    https://recall.report/device/z-1291-2022/
    Recall Initiation Date: 20220602: Recalling Firm: Wright Medical Technology, Inc. Initial Notification : Letter: Similar To: GE Healthcare, LLC Recall …

Wright Medical Technology, Inc. Recall 89086 – Product Safety …

    https://recall.report/device/z-0401-2022/
    Recall Number. Z-0401-2022. Event ID. 89086. Event Description. Wright Medical Technology Inc. CHARLOTTE MTP Hex Screw, Model #41122718, 2.7mm x …



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