FDA Issues Class I Recalls for Breathing Circuits, Catheters, and Spinal Cord Stimulators

The U.S. Food and Drug Administration has identified Class I recalls for several medical devices, including Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits, certain reprocessed electrophysiology and ultrasound catheters by Medline, and all unused Infinion CX Leads by Boston Scientific. Class I recalls are the most serious type, indicating a reasonable probability of serious adverse health consequences or death.