Device evidence

device-recall:cfres:176306

Custom Procedure Kit, Vein Kit, Product Code/REF: K12T-10167, single use, RX Only, Sterile EO, UDI: (01) 00884450390580

Official recall number

Z-0027-2020

Evidence summary

Product code: OES
Recall status: Terminated
Event initiated: October 26, 2018
Root cause: Error in labeling
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0027-2020