Fda Medical Device Recalls 2010

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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

Medical Device Recalls - Food and Drug Administration

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

Recalls, Market Withdrawals, & Safety Alerts | FDA

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

A Terminated Recall is a recall where the FDA has determined that all …

Recalls, Corrections and Removals (Devices) | FDA

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

Medical Device Recalls - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/resCollection_2.cfm?ID=92118

April 26, 2010: Create Date: September 13, 2010: Recall Status 1: Terminated 3: Recall Number: Z-2409-2010: Recall Event ID: 55876: Product: NexGen …

Medical Device Recalls - accessdata.fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&event_id=55535&productdescriptiontxt=&productcode=&rootCauseText=¢erclassificationtypetext=&recallnumber=&postdatefrom=&postdateto=&productshortreasontxt=&firmlegalnam=&PMA_510K_Num=&pnumber=&knumber=&sortcolumn=cdd

Related Medical Device Recalls: ... Recall Class. FDA Recall Posting Date. Recalling Firm. Z-1816-2010 - Excyte Slider Barcode Tube Adapter used with Excyte Vacuum or Non …

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) …

GE HealthCare Recalls Nuclear Medicine Systems for …

https://www.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 …

Medical Device Recalls - accessdata.fda.gov

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?start_search=1&knumber=K220287

Medical Device Recalls. FDA Home; Medical Devices; Databases - 1 result found ... FDA Recall Posting Date. Recalling Firm. Invisalign Express 10 REF 8512 …

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Medical Device Recalls | FDA

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

Medical Device Recalls - accessdata.fda.gov

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

GE HealthCare Recalls Nuclear Medicine Systems for …

Medical Device Recalls - accessdata.fda.gov

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