FDAJanuary 2, 2020device

Central Venous Catheters are indicated for the assessment of hemodynamic status through right atrial, right ventricular, and pulmonary artery and/or wedge pressure monitoring for patients. Model # 41401-23.

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

The hazard

Inability for the guidewire to pass through the needles included with the catheter kits.

What to do

FDA enforcement status: Terminated

Brands named

icu medicalicu

UPCs

10840619044098

Recall history

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

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