Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:118594

TRUE Dilatation Balloon Valvuloplasty Catheter, REF Numbers: 02045-11, 02245-12, 02445-12, and 02645-13; Sizes: 20mm x 4.5cm, 22mm x 4.5cm, 24mm x 4.5cm, and 26mm x 4.5cm; Intended to be used for balloon aortic valvuloplasty.

Official recall number

Z-1566-2013

Evidence summary

Product code
OZT
Recall status
Terminated
Event initiated
March 18, 2013
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1566-2013

Field note

Send feedback

We'll only use this to respond to your feedback.