OriGen Biomedical, Inc. recalls Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO
Recalled Product
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO
Hazard / Issue
The catheter failed the endotoxin testing.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI: 00816203022059, lot N18687-1
View official government recall
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