Regulators Flag 184 Serious Injuries Tied to a Swallowed Capsule Used in Routine Acid Reflux Testing
The FDA issued a safety alert for Medtronic's Bravo CF capsule delivery devices, reporting 184 serious injuries due to a failure in capsule attachment or detachment. The alert covers unused inventory with expiration dates on or before October 20, 2027. Medtronic has recalled affected lots and is replacing them. Patients scheduled for reflux testing should verify their clinic's inventory.







