Oscor, Inc. recalls AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 -
Recalled Product
AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various types of pacing leads and catheters.
Hazard / Issue
Potential for open seal on sterile product
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: GUDID: 25051684026298; Lot Number DP-11759
View official government recall
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