FDAFebruary 21, 2022device

Empower Introducer Sheath with Hydrophilic Coating 21F x 56cm Model: 668782-100 (US)

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

The hazard

Non-intended glue from the hub/shaft bond on the inside ID of the catheter shaft may cause Embolism leading to peripheral ischemia

What to do

FDA enforcement status: Terminated

Brands named

freudenberg medicalfreudenberg

UPCs

00850004312001

Recall history

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

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