Feth-R-Kath Catheter recall
Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to…
Why was Feth-R-Kath Catheter recalled?
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot Numbers: 11247915, 11248510, 11248553, 11248938, 11248985, 11249049
- 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…
- Recalling firm
- Epimed International, Inc.
- Quantity
- 5835 units
- Distribution
- US Nationwide distribution
- Recall date
- March 24, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)