Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer coating of the catheter may deteriorate and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Epimed International, Inc. directly.
Affected Products
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
Quantity: 5835 units
Why Was This Recalled?
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Epimed International, Inc.
Epimed International, Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report