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Class 2 Device Recall EXCELSIOR MEDICAL LLC

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=194495
    Recall Status 1: Open 3, Classified: Recall Number: Z-1596-2022: Recall Event ID: 90336: 510(K)Number: K133446 Product Classification: Heparin, vascular access flush - Product Code NZW: Product:...

Class 2 Device Recall Excelsior Medical Inc. - Food and …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=146056
    Excelsior Medical Corp 1933 Heck Ave Neptune NJ 07753-4428: For Additional Information Contact: Mr. John Linfante 732-643-6088 Manufacturer Reason for …

MAUDE Adverse Event Report: EXCELSIOR MEDICAL …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=15543647&pc=NZW
    HEPARIN FLUSH HEPARIN, VASCULAR ACCESS FLUSH. Back to Search Results. Model Number EMZE060055. Device Problem Packaging Problem (3007) Patient …

International Medical Devices Database

    https://medicaldevices.icij.org/devices/usa-general-hospital-and-personal-use-devices-device-recall-heparin-lock-flush
    Product Description. Heparin Lock Flush Solution 100 Unit/mL, USP || 3 ml, 4 ml, 5mL, 6 ml fill in a 10 ml Flush Syringe ZR || Excelsior Medical Neptune, NJ 07753 || (800) 487-4276 …

International Medical Devices Database

    https://medicaldevices.icij.org/events/usa-device-recall-heparin-lock-flush
    Excelsior Medical sent an "URGENT MEDICAL DEVICE RECALL" letter dated May 4, 2012 to all affected customers. The letter identifies the product, problem, and actions to …

SCA Pharmaceuticals (SCA) Is Issuing a Voluntary …

    https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sca-pharmaceuticals-sca-issuing-voluntary-nationwide-recall-heparin-sodium-compounded-products-due
    SCA Pharmaceuticals (SCA) Is Issuing a Voluntary Nationwide Recall of Heparin Sodium Compounded Products Due to Incorrect Preservative (Benzyl Alcohol) …

Class 2 Device Recall Syrex - Food and Drug …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=47264
    Class 2 Device Recall Syrex FDA Home Medical Devices Databases 510 (k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards …

ZR Flush Syringes | Excelsior Medical, LLC

    http://swabflush.excelsiormedical.com/zr-flush-syringes/
    * Data on file at Excelsior Medical, LLC ** Codes E0500 55 (10U/mL heparin 5mL in 10mL syringe) and E0600 55 (100U/mL heparin 5mL in 10mL syringe) have a shelf life …

Medical Device Recalls

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=47264
    Excelsior Medical Corp 1923 Heck Ave Neptune NJ 07753-4428: For Additional Information Contact: Himanshu Naik 732-643-6080 Manufacturer Reason for …

Excelsior Medical Heparin Recall | Day of Difference

    https://dayofdifference.org.au/e-medical/excelsior-medical-heparin-recall.html
    Excelsior Medical Heparin Recall | Day of Difference All information about Excelsior Medical Heparin Recall At dayofdifference.org.au you will find all the information about …



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