Description: Medline updates use instructions for Electronic Homecare Beds due to risk of electrical fires and entrapment.

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/electronic-homecare-bed-correction-medline-updates-use-instructions-homecare-beds
Date: 2026-02-13

Description: AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information.

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/emergency-response-safety-kit-recall-airlife-removes-certain-broselow-pediatric-emergency-rainbow
Date: 2026-02-11

Glucose Monit

Description: FT. LAUDERDALE, FL) – February 6, 2026 – Trividia Health, Inc., announced today that it is initiating a labeling correction which requires a modification of the Owner’s Booklets/System Instructions for Use for all TRUE METRIX, TRUE METRIX AIR, TRUE METRIX GO, and TRUE METRIX PRO Blood

Link: http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/trividia-health-inc-initiates-labeling-correction-all-true-metrixr-blood-glucose-monitoring-systems
Date: 2026-02-06

Description: Certain Abbott Diabetes Care Continuous Glucose Monitor sensors may incorrect or lower than actual glucose readings

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/glucose-monitor-sensor-recall-abbott-diabetes-care-removes-certain-freestyle-libre-3-and-freestyle
Date: 2026-02-05

Description: MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/detachable-coil-system-recall-jj-medtechcerenovus-inc-remove-cerepak-detachable-coil-system
Date: 2026-02-05

Description: Certain Abbott Diabetes Care Continuous Glucose Monitor sensors may incorrect or lower than actual glucose readings

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/glucose-monitor-sensor-recall-abott-diabetes-care-removes-certain-freestyle-libre-3-and-freestyle
Date: 2026-02-04

Description: The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift.

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-heart-pump-issue-abiomed
Date: 2026-02-03

Description: Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.

Link: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/early-alert-insufflation-unit-issue-olympus
Date: 2026-01-22