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Class 2 Device Recall DePuy Synthes - Food and Drug …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=182662
    DePuy Synthes issued Urgent Medical Device Removal letter dated July 21, 2020 stating reason for recall, health risk and action to take: Please take the following actions: 1. Immediately examine...

2022 Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
    2021 Medical Device Recalls Subscribe to Medical Device Safety and Recalls Sign up to receive email updates on medical device recalls, safety communications, and other …

Class 2 Device Recall Synthes Electric Pen Drive (EPD) …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=132629
    Class 2 Device Recall Synthes Electric Pen Drive (EPD) System. Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw …

Class 3 Device Recall DePuy Synthes SYNMESH - Food …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=184002
    Recall Number: Z-0403-2021: Recall Event ID: 86545: 510(K)Number: K983766 K003275 Product Classification: Spinal vertebral body replacement device - …

Class 2 Device Recall Synthes XRL Medium TrialCentral …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=126770
    Action Required: Synthes has record that your facility has the product(s) subject to this recall. Synthes asks that you review your inventory and immediately …

Class 2 Device Recall Synthes Radial Head Prosthesis …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=152471
    Synthes (USA) Products LLC 1301 Goshen Pkwy West Chester PA 19380-5986: Manufacturer Reason for Recall: There is the possibility that the radial stem may …

Cleaning & Sterilization Guidelines | DePuy Synthes - J&J MedTech

    https://www.jnjmedtech.com/en-US/service-details/cleaning-sterilization-guidelines/depuy-synthes
    The proper processing of devices is paramount to ensuring patient safety. Since cleaning and sterilization instructions vary among device manufacturers, health care facilities must …

Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
    If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …

DePuy Orthopaedics | DePuy Synthes

    https://www.jnjmedtech.com/en-US/companies/depuy-synthes
    DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, in addition to the VELYS™ Digital …

Recall of Device Recall DePuy Synthes Titanium Recon …

    https://medicaldevices.icij.org/events/usa-device-recall-depuy-synthes-titanium-recon-screws
    International Medical Devices Database Events Recall of Device Recall DePuy Synthes Titanium Recon Screws According to U.S. Food and Drug Administration, this recall …



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