Alcon Research, LTD. recalls Constellation Procedure Pak
Recalled Product
Constellation Procedure 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. 8065750958; Product Code 100007216; UDI-DI: 380657509584; Lots 14XM2J, 14Y1H6, 150HYJ, 150HYK, 151R72, 152CH0, 15309X, 156HWN, 15A13R, 15A13T, 15CF2X, 15CF2Y, 15CF30, 15CJ47, 15CJ48, 15CWAM, 15CWAN, 15D649.
View official government recall
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