FDAOctober 11, 2019device

The PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-compliant balloon systems mounted at the distal tip (balloon within a balloon design). The catheter is available in various working lengths and appropriate balloon diameters and lengths. The balloon has r...

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

The hazard

Peripheral Dilation Catheters that were E-Beam Sterilized were inadvertently mislabeled with EO sterilized labels.

What to do

FDA enforcement status: Terminated

Brands named

nucryo vascularnucryo

Recall history

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

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The PolarCath Balloon Catheter consists of a coaxial catheter shaft with two concentric, non-compliant balloon systems mounted at the distal tip (balloon within a balloon design). The catheter is available in various working lengths and appropriate balloon diameters and lengths. The balloon has r... — Recall Details · AllClear