Device evidence

device-recall:cfres:200959

Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK, REF 89-7102; b) CHOLANGIOGRAPHY KIT, REF 89-7322; c) CATH LAB PACK, REF 89-9183

Official recall number

Z-2090-2023

Evidence summary

Product code: OEQ
Recall status: Open, Classified
Event initiated: May 30, 2023
Root cause: Process control
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-2090-2023