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Applied Medical Recalls Python Embolectomy, BARD …

    https://www.fda.gov/medical-devices/medical-device-recalls/applied-medical-recalls-python-embolectomy-bard-embolectomy-and-otw-latis-cleaning-catheters-due
    Applied Medical is recalling their Python Embolectomy Catheters, Bard Embolectomy Catheters, and OTW Latis Cleaning Catheters because there is a risk of the catheter tip detaching during use. If the tip detaches, pieces of the catheter could break off into the patient’s body. If this occurs, there is also the potential for serio… See more

BARD® MARQUEE® Disposable Core Biopsy …

    https://www.bd.com/documents/alerts/PI_Bard-Marquee-disposable-core-biopsy-instruments-and-kits-recall_CL_EN.pdf
    Bard Peripheral Vascular, Inc. 850 W. Rio Salado Parkway, Suite 100 Tempe, AZ, 85281 bd.com URGENT MEDICAL DEVICE RECALL BARD® MARQUEE® Disposable Core …

Bard convinces U.S. appeals court to revive medical-injection …

    https://www.reuters.com/legal/bard-convinces-us-appeals-court-revive-medical-injection-device-patents-2023-02-17/
    18 hours ago · Becton Dickinson's C.R. Bard Inc on Friday won a ruling from a U.S. appeals court reinstating three patents related to its PowerPort devices for delivering repeated …

Medical Device Recalls | FDA

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

Bard convinces U.S. appeals court to revive medical-injection …

    https://finance.yahoo.com/news/bard-convinces-u-appeals-court-212447212.html
    The decision from the Washington, D.C.-based U.S. Court of Appeals for the Federal Circuit revives a long-running infringement lawsuit Bard brought against …

URGENT MEDICAL DEVICE RECALL - BD

    https://www.bd.com/documents/alerts/PI_PowerPort-duo-MRI-Implantable-Port-Kits-recall_CL_EN.pdf
    This letter is to inform you of a Voluntary Medical Device Product Recall being conducted by Bard Access Systems, Inc., a wholly owned subsidiary of Becton, Dickinson and …

Bard Mesh - BD

    https://www.bd.com/en-us/products-and-solutions/products/product-families/bard-mesh
    Overview. The Gold Standard, Monofilament, Polypropylene Mesh. With more than 50 years of clinical experience, Bard ® Mesh is the Gold Standard product to be used in a …

What hernia mesh has been recalled? - Top …

    https://topclassactions.com/lawsuit-settlements/medical-devices/what-hernia-mesh-has-been-recalled/
    Brands that have recalled hernia mesh products include Atrium Medical, Bard Davol, and Ethicon. Between 2005 and February 2019, more than 211,000 …

2022 Medical Device Recalls | FDA

    https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
    11/01/22. Philips Respironics Recalls Certain Masks for BiPAP, CPAP Machines Due to Safety Issue with Magnets That May Affect Certain Medical Devices. 10/18/22. Jiangsu …

Class 2 Device Recall BardPort M.R.I. Implantable Port

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=179828
    Once the Recall and Effectiveness Check Form has been completed and emailed to [email protected] or faxed to BPV at 1-800-994 …



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