Medical Equipment Recalls

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...

2021 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2021-medical-device-recalls

Dec 16, 2021

2022 Medical Device Recalls | FDA

https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls

Vyaire Medical Recalls bellavista 1000 and 1000e Series Ventilators Due to Issues with Software Configurations 02/17/22 Empowered Diagnostics Recalls COVID-19 Tests due …

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/res.cfm

Recalls.gov

https://www.recalls.gov/medicine.html

The Food and Drug Administration (FDA)has jurisdiction over recalls involving the following: drugs vaccines medical devices other biologics blood and plasma products veterinary …

Seven serious medical device failures that …

https://www.nsmedicaldevices.com/analysis/medical-device-failures-fda-recalls/

In January 2016 US medical device company Verathon recalled more than 7,700 of its GlideScope titanium single-use laryngoscope devices for viewing and videoing the vocal cords. …

Protect Yourself from Recalled Products | USAGov

https://www.usa.gov/recalls

NHTSA.gov publishes safety information on vehicles and equipment, such as children's car seats. FSIS.USDA.gov lists meat, sausage, poultry, and processed egg …

Recalls | CPSC.gov - U.S. Consumer Product Safety …

https://www.cpsc.gov/Recalls

WeeSprout Recalls Baby Sleep Sacks Due to Choking Hazard (Recall Alert) Hazard: The zipper can detach from the sleep sack, posing a choking hazard. Remedy: …

VHA Directive 1068 Removal of Recalled Medical …

https://www.va.gov/vhapublications/ViewPublication.asp?pub_ID=8892

Product Recall. A product recall is a method for removing products from use that are in violation of laws administered by the FDA or otherwise deemed defective or potentially …