FDAJuly 13, 2016device

6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal femoral arterial and femoral venous access sites while reducing times to hemostasis and ambulation in patients who have undergone diagnostic or inte...

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

The hazard

A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.

What to do

FDA enforcement status: Terminated

Brands named

accessclosure inc a cardinal healthaccessclosureaccessclosure inc

Recall history

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

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