medical Class II Updated 2018-10-24

OriGen Biomedical, Inc. recalls Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO

Recalled Product

Reinforced Dual Lumen Cannula, 23Fr., REF: VV23F, Sterile EO Indications: The OriGen Reinforced Dual Lumen Cannula is indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures.

Hazard / Issue

These catheters may have the following deficiencies: 1) barium sulfate omission, and 2) actual catheter tip length is one centimeter shorter than printed on the tip

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 00816203022103, Lot: N18431, N18431-1
View official government recall

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