Device evidence

device-recall:cfres:211381

Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF, REF DYNJ39461J; 2) NEURO BASIN KIT, REF DYNJ80200B.

Official recall number

Z-0787-2025

Evidence summary

Product code: KDD
Recall status: Open, Classified
Event initiated: November 21, 2024
Root cause: Nonconforming Material/Component
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0787-2025