Medical Device Recalls 2011

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 for November 2011 - MassDevice

https://www.massdevice.com/medical-device-recalls-november-2011/

Dec 1, 2011

Medical device recalls for December 2011 - MassDevice

https://www.massdevice.com/medical-device-recalls-december-2011/

Jan 2, 2012

GE HealthCare Recalls Nuclear Medicine Systems for …

https://cacmap.fda.gov/medical-devices/medical-device-recalls/ge-healthcare-recalls-nuclear-medicine-600800-series-systems-risk-detector-fall-may-injure-patients

GE HealthCare Recalls Nuclear Medicine 600/800 Series Systems for Risk of Detector Fall That May Injure Patients The FDA has identified this as a Class I recall, …

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

Either of these recall issues can cause delay of therapy, interruption of therapy, or under-delivery of medication, which all have the potential to cause serious …

GE HealthCare recalls scanner for patient crushing risk

https://www.massdevice.com/ge-healthcare-recalls-scanner-for-patient-crushing-risk/

2 days ago · The recall includes the NM 830 and 830 ES as well as the NM/CT 850, 850 ES, 860, 860 ES, 870 CZT, 870 DR and 870 ES. GE Healthcare distributed the affected …

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.

Medical Device Safety | FDA - U.S. Food and Drug …

https://www.fda.gov/medical-devices/medical-device-safety

Medical Device Recalls; Letters to Health Care Providers; Medical Device Bans; Medical Device Reporting (MDR): How to Report Medical Device Problems; Reporting …