Class I recall

FDA
MedTech

FDA boosts Philips recall of hospital, home ventilator software

The agency labeled the recall effort as Class I, its most serious, and said it received reports of nine injuries and one death.
Conor Hale Oct 2, 2024 3:00pm
FDA stop sign

FDA boosts 3 recalls of Smiths Medical ventilators, trach tubes

Sep 23, 2024 4:00pm
FDA stop sign

FDA boosts Medtronic scope recall over battery explosion risk

Sep 6, 2024 12:27pm
FDA

The FDA calls them 'recalls.' Yet many devices remain in use

Aug 19, 2024 9:15am
Medtronic headquarters

FDA issues Class 1 recall for Medtronic's nerve monitoring tech

Aug 8, 2024 2:30pm
FDA stop sign

FDA boosts Medtronic endotracheal tube recall

Jul 10, 2024 11:15am