Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1276-2021 — 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

U.S. FDA — Device Enforcement · United States · 2021-02-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1276-2021
Date of alert
2021-02-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Epimed International, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
11247915
Reported risk: Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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