FDASeptember 20, 2022device

Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling UPN: H7...

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

The hazard

Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, and Post Operative Care of the implantable port, failure to follow the Instructions for Use may result in patient injury.

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

15051684018357

Recall history

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

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