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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:185227

INJECTOR FORCEMAX UP 2.8MMCH 23G 4MM, model no. NM-400L-0423 - Product Usage: Used with endoscopes to perform endoscopic injection for the treatment of esophageal and gastric varices and for submucosal injection in the digestive tract.

Official recall number

Z-0994-2021

Evidence summary

Product code
FGX
Recall status
Terminated
Event initiated
January 04, 2021
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0994-2021