Epimed International, Inc. recalls Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural…
- Recall date
- February 1, 2021
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1276-2021
- FDA classification
- Class II
- Brand / firm
- Epimed International, Inc.
- Sold / distributed
- US Nationwide distribution
Why it was recalled
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
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