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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 they could cause serious health...

GE HealthCare Recalls Nuclear Medicine Systems for …

    https://cacmap.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients
    See Medical Device Recall Database entry for more information. Distribution Dates: April 1, 2018 to December 16, 2022; Devices Recalled in the U.S.: 688; Date …

BD Provides Update on Previously Disclosed Recall of …

    https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-provides-update-previously-disclosed-recall-bd-alaris-system-hardware
    BD initiated the voluntary recall to notify customers of the potential for four hardware situations that may result in the infusion pump not operating as expected. BD …

Medical Device Recalls - Food and Drug Administration

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&event_id=&productdescriptiontxt=¢erclassificationtypetext=&recallnumber=&postdatefrom=&postdateto=&productshortreasontxt=&firmlegalnam=DePuy&knumber=&pnumber=
    Medical Device Recalls. BIOSTOP G BIORESORBABLE CEMENT …

4 Things Healthcare Facilities Should Know About Medical …

    https://hitconsultant.net/2021/09/13/medical-device-recalls-tips/
    Recall notices don’t go to the right person. After a hospital purchases medical devices and …

Knee Replacement Lawsuits | 2022 …

    https://www.consumersafety.org/medical-device-lawsuits/knee-replacement/
    According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components between 2003 and 2019. The companies with …

Seven serious medical device failures that …

    https://www.nsmedicaldevices.com/analysis/medical-device-failures-fda-recalls/
    Medical device failures can have adverse consequences for healthcare professionals, as well as patients, in certain cases. Class I medical device recalls …

Recalls

    https://bdx.force.com/CC360/s/parentrecall
    Durability issues may be experienced with certain exterior plastic cases and handles on the Alaris™ Syringe Module 8110 & Alaris™ PCA Module 8120. …

Recall | Stryker

    https://www.stryker.com/us/en/about/contact/recall.html
    Recall. Send an email to us. This contact form is for recall questions only. For other inquiries, please review this page for additional points of contact. recall. To request …

Medical Device Recalls - Food and Drug Administration

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm
    This database contains Medical Device Recalls classified since November 2002. Since January 2017, it may also include correction or removal actions initiated by …



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