Merit Medical Systems, Inc. recalls Custom Procedure Kit, Vein Kit, Product Code/REF: K12T-10167
Recalled Product
Custom Procedure Kit, Vein Kit, Product Code/REF: K12T-10167, single use, RX Only, Sterile EO, UDI: (01) 00884450390580
Hazard / Issue
Labeling error; It was identified that a Procedure Kit/Tray contained incorrect latex labeling information (i.e. indicated Latex Free)
Issued by
FDA
Affected States: VA, IL
Lot/Code Info: Catalog # K12T-10167, Lot # K12T-10167, Use By: 2018-11-05
View official government recall
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