Fda Medical Device Recalls 2009

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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 ...

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm

UPDATE: Certain Philips Respironics Ventilators, BiPAP …

https://www.fda.gov/medical-devices/safety-communications/update-certain-philips-respironics-ventilators-bipap-machines-and-cpap-machines-recalled-due

Philips recalled the following devices made between 2009 and April 26, 2021: ... More information on medical device recalls, including What is a Medical Device Recall, is …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/textsearch.cfm

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?start_search=1&event_id=50901

Related Medical Device Recalls 1 2 3 ... Product Description. Recall Class. FDA Recall Posting Date. Recalling Firm. Z-1354-2009 - Accolade TMZF Hip Stem; Hydroxylapatite …

Recalls, Market Withdrawals, & Safety Alerts | FDA

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

The Recalls, Market Withdrawals & Safety Alerts are available on FDA’s website for three years before being archived. To search archived content, visit Search FDA …

Recalls, Corrections and Removals (Devices) | FDA

https://www.fda.gov/medical-devices/postmarket-requirements-devices/recalls-corrections-and-removals-devices

Recall means a firm's removal or correction of a marketed product that the FDA considers to be in violation of the laws it administers and against which the agency would initiate legal …

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&event_id=52076

Medical Device Recalls. FDA Home; Medical Devices; Databases - 1 to 10 of 10 Results Related Medical Device Recalls ... Recall Class. FDA Recall Posting Date. …

2023 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2023-medical-device-recalls

2022 Medical Device Recalls. Device Name. Date. Smiths Medical Recalls Certain CADD System Administration Sets and Cassette Reservoirs for Issues Causing …

U.S. FDA classifies recall of Philips' respiratory devices as most ...

https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-classifies-recall-philips-respiratory-devices-most-serious-2023-02-16/

1 day ago · Follow. Feb 16 (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of Dutch medical devices maker Philips' (PHG.AS) …

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Medical Device Recalls | FDA

Medical Device Recalls - Food and Drug Administration

UPDATE: Certain Philips Respironics Ventilators, BiPAP …

Medical Device Recalls - Food and Drug Administration

Medical Device Recalls - Food and Drug Administration

Recalls, Market Withdrawals, & Safety Alerts | FDA

Recalls, Corrections and Removals (Devices) | FDA

Medical Device Recalls - Food and Drug Administration

2023 Medical Device Recalls | FDA

U.S. FDA classifies recall of Philips' respiratory devices as most ...

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