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Draeger Recalls SafeStar 55 Filters For Possible …

    https://www.fda.gov/medical-devices/medical-device-recalls/draeger-inc-recalls-safestar-55-breathing-system-filters-possible-obstructions-may-block-oxygen-flow
    On May 16, 2022, Draeger issued an Urgent Medical Device Recall letter to customers who may have received filters from the affected lot. The letter requested customers to: 1. Check stock for filters with the lot number LT2103 2. Segregate/quarantine any filters with the lot number listed. 3. … See more

Class 1 Device Recall Drager SafeStar 55, Catalog No.

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=193712
    Action. The firm distributed a notification titled "URGENT MEDICAL DEVICE RECALL" by mail on 05/16/2022, in which it informed customers of the voluntary recall of …

Class 2 Device Recall Draegar - Food and Drug …

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=192260
    Recall Status 1: Open 3, Classified: Recall Number: Z-0870-2022: Recall Event ID: 89702: 510(K)Number: K093633 Product Classification: ... Draeger Medical, …

Draeger has a serious ventilator filters recall - MassDevice

    https://www.massdevice.com/draeger-fda-ventilator-filter-recall/
    The FDA today issued a notice confirming that a recall of ventilator filters from Draeger is Class I, the most serious kind. Draeger’s SafeStar 55 breathing system …

Draeger Medical recalls single-use breathing circuits

    https://www.medtechdive.com/news/draeger-medical-recalls-single-use-breathing-circuits/546935/
    Dive Brief: Draeger Medical is recalling its VentStar and ID Breathing Circuits and Anesthesia Sets due to the risk of a short circuit if the devices are not …

Draegar Medical Systems, Inc. - 596529 - 01/17/2020 | FDA

    https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/draegar-medical-systems-inc-596529-01172020
    January 17, 2020. Dear Mr. Dräger: The United States Food and Drug Administration (FDA) conducted an inspection of your firm’s medical device operations, …

Coronavirus (COVID-19 or nCoV) - Dräger's Important

    https://www.draeger.com/en-us_us/Novel-Coronavirus-Outbreak
    Customer Letter: Reprocessing and Handling of Medical Supply Systems/Medical Lights The following information and recommendations are targeted for …

Draeger Medical, Inc. Recall 87267 – Product Safety Recalls

    https://recall.report/device/z-1180-2021/
    Recall Number. Z-1180-2021. Event ID. 87267. Event Description. ID Circuit Basic (N) 180-Drager Breathing Circuits/Anesthesia Sets Order Number: MP01327 - …

Draeger Medical, Inc. Recall 88635 – Product Safety Recalls

    https://recall.report/device/z-0109-2022-2/
    Draeger Medical, Inc. Recall 88635. Description: Babylog VN500 Ventilator with Installed CO2 Measurement Option-intended for the ventilation of neonatal patients …

Draeger Medical, Inc. - International Medical Devices …

    https://medicaldevices.icij.org/manufacturers/u-s-food-and-drug-administration-draeger-medical-inc-draeger-medical-inc-3135-quarry-rd-telford-pa-18969-1042
    Draeger Medical, Inc. Manufacturer Address. Draeger Medical, Inc., 3135 Quarry Rd, Telford PA 18969-1042. Manufacturer Parent Company (2017) Stefan Dräger GmbH. …



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