Reported Mar 24, 2021 · Terminated
Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural…
Epimed International, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Epimed International, Inc. · 141 Sal Landrio Dr · Johnstown, NY · 12095-3835
Is this the product you have?
- Feth-R-Kath Catheter, 19g x 24"
- Intended UseRadlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to placement of 72 hours or less
- Lot codes and dates
- Lot Numbers
112479151124851011248553112489381124898511249049
- Lot Numbers
- Amount recalled
- 5835 units
Where it was sold
- Nationwide
Why it was recalled
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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