Back to RecallTracker
Health Canada Medical devices

EsoFLIP Dilation Catheter 30mm

Issued May 3, 2024
Issue
Medtronic has received complaints of ES-330 catheters measuring diameters that are significantly (more than 50%) lower than actual. The failure mode may be reported as "failed precheck", "incorrect distensibility reading", "no distensibility value displayed", "adverse event without identified device or use problem", or "diameter incorrect." Medtronic Lafayette returned product analysis lab testing of unused, returned ES-330 catheters showed saline conductivity that is approximately 10 times lower than specification. The ES-330 saline conductivity specification is 2.25 mS/cm. The saline conductivity of multiple unused, returned ES-330 catheters had saline conductivity at or near 0.25 mS/cm. Recall start date: April 25, 2024
Hazard description
Performance
Product
Product name
EsoFLIP Dilation Catheter 30mm
Reference
ID
RA-75471