FDAFebruary 1, 2021device

Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to placement of 72 hours or less

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

The hazard

Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off

What to do

FDA enforcement status: Terminated

Brands named

epimed

Recall history

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

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