Device evidence

device-recall:cfres:124229

Viscocel and Viscocel Plus. These products are intraocular fluid devices consisting of non-gaseous fluid intended to be introduced into the eye to aid performance of surgery, such as to maintain anterior chamber depth, preserve tissue integrity, protect tissue from surgical trauma, or function as a tamponade during retinal reattachment.

Official recall number

Z-0531-2014

Evidence summary

Product code: LZP
Recall status: Terminated
Event initiated: November 25, 2013
Root cause: No Marketing Application
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0531-2014