AMSCO Evolution Prevacuum Steam Sterilizer & AMSCO Evolution SFPP Steam Sterilizer (2019-10-23)

The detector on the Forte Gamma Camera System has the potential to become detached without warning which could result in a serious injury or death.

Abbott is recalling their CentriMag System due to a calibration system error resulting from electromagnetic interference (EMI) that may cause low or no flow from the device, the console screen to blank, and various inaccurate alarms.

The remote controllers of some Medtronic MiniMed insulin pumps are vulnerable to cybersecurity risks. Unauthorized persons could record and replay the wireless communication from the remote to the MiniMed insulin pump leading to the administration of one ore more unintended boluses of insulin.

The FDA posts Medical Device Safety Communications to describe the FDA’s current analysis of an issue and contain specific regulatory approaches and clinical recommendations for patient management.

Statistiques des urgences prises en charges Octobre 2019