Day

August 5, 2024
05
Aug

FDA Recall: Incorrect or Delayed Patient Treatment May Result from Incorrect Updated Software Options

August 5, 2024
Company: Philips North America Llc Date of Enforcement Report: 8/5/2024 Class II PRODUCT IntelliVue Patient Monitor MX400 with L.x and M.x; K.x provided with L.x entitlements Model Number: 866060. Indicated for use by health care professionals for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates. Recall...
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