Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:128389

Baxter, MiniCap with Povidone-Iodine solution, 5C4466P. For dialysis.

Official recall number

Z-1945-2014

Evidence summary

Product code
KDI
Recall status
Terminated
Event initiated
July 08, 2013
Root cause
Packaging change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1945-2014