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Epimed International, Inc. recalls Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidu
Recalled March 24, 2021 · FDA recall Z-1276-2021 · Epimed International
Hazard
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off · FDA Class II
Units
5835 units
Sold at
US Nationwide distribution
Description
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
Product
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
Manufacturer(s)
Epimed International, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →