Drug RecallsUpdate On Device Failure Associated with Getinge’s Maquet/Datascope Intra-Aortic Balloon Pumps – Letter to Health Care Providers Posted on by Editor Date: 12/22/2021 Product type: Medical Device USA-FDA Link: https://www.fda.gov/medical-devices/letters-health-care-providers/update-device-failure-associated-getinges-maquetdatascope-intra-aortic-balloon-pumps-letter-health Getinge’s Maquet/Datascope IABP Devices: Update on Device Failure – Letter to Health Care Providers Possible False RPR Reactivity with BioPlex 2200 Syphilis Total & RPR Test Kit Following a COVID-19 Vaccine – Letter to Clinical Laboratory Staff and Health Care Providers
