Medtronic announced a recall of certain capsule delivery devices after reports of 33 serious injuries. The U.S. Food and Drug Administration (FDA) published an early alert for this recall on June 25, 2025.
The specific nature of the device and the injuries were not detailed, but the number of reported serious injuries indicates a significant product safety concern. No deaths have been associated with this particular problem.
This recall represents another product safety challenge for Medtronic, potentially impacting its reputation and requiring corrective actions. It underscores the ongoing regulatory scrutiny faced by medical device manufacturers.
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