FDAJanuary 17, 2017device

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Clamping the clear tube very close to the blue hub may cause a localized adhesive failure in the bond between the clear tube and the molded hub. Forcefully rotating the clamp while it is in place may potentially cause an immediate disconnect of the clear tube or lead to a later fatigue failure of the adhesive bond, with subsequent clear tube disconnect from the hub.

What to do

FDA enforcement status: Terminated

Brands named

origen biomedicalorigen

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F — Recall Details · AllClear