Medical Device Recalls 2010

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

Recalls, Corrections and Removals (Devices) | FDA

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

Medical device recalls due to software …

https://www.statista.com/statistics/618218/medical-device-software-related-recalls/

Number of medical device recalls due to software issues in the U.S. 2010-2018 Published by Conor Stewart Conor Stewart Research expert covering health & …

Medical Device Labeling/Packaging Recalls …

https://www.innovatum.com/2016/05/medical-device-labeling-packaging-recalls/

This analysis demonstrates recall issues related to the labeling and packaging of medical devices …

Causes for medical device recalls U.S. 2010-2015 | Statista

https://staginges.statista.com/estadisticas/618240/medical-device-recall-causes/

Causes for medical device recalls in the U.S. 2010-2015. Publicado por Statista Research Department , 18 jul. 2016. This statistic shows the leading causes of …

Smiths Medical Recalls Certain CADD System …

https://cacmap.fda.gov/medical-devices/medical-device-recalls/smiths-medical-recalls-certain-cadd-system-administration-sets-and-cassette-reservoirs-issues

Smiths Medical is recalling certain CADD Administration Sets and Medication Cassette Reservoirs for two potential issues: Tubing occlusion prevents delivery or …

GE HealthCare Recalls Nuclear Medicine 600/800 …

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 …

Philips recalls certain reworked Trilogy, Garbin ventilators

https://www.massdevice.com/philips-recalls-reworked-trilogy-garbin-ventilators/

1 day ago · The FDA notice includes devices distributed between March 1, 2022, and Sept. 6, 2022. Devices recalled in the U.S. total 13,811 since Philips initiated the recall on Dec. …

Medical Device Recalls

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

Recalling Firm. 13. 14. Invisalign Express 10 REF 8512 Invisalign System Comprehensive REF 9000 Invisalign System ... 15. 2. 01/26/2023. Align Technology Inc.