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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115620

Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9. Product Usage: The catheter introducer sheath kit provides access to the central venous circulation to facilitate catheter and guidewire insertion. The Proplege coronary sinus catheter provides retrograde cardioplegia during cardiopulmonary by-pass surgery.

Official recall number

Z-1322-2013

Evidence summary

Product code
DWF
Recall status
Terminated
Event initiated
January 25, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1322-2013

Field note

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