medical Class II Updated 2023-08-23

Alcon Research, LTD. recalls Legion FMS Pak

Recalled Product

Legion FMS Pak


Hazard / Issue

Reports of patient injury during use in procedures due to potential for plastic debris from over-tightening with included plastic wrench.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Catalog No. 8065753164, 8065753165, 8065753166; Product Code 100205822, 100207728, 100207729; UDI-DI: 380657531646, 380657531653, 380657531660; Lots 14YTR7, 153UW1, 156YMH, 157R2M.
View official government recall

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