FDA Device 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 li…
- FDA Device
- Class II
- terminated
- Published 2021-03-24
On 2021-03-24 the FDA classified a Class II recall of Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is li… by Epimed International, citing outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1276-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-02-01 |
| Published | 2021-03-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Epimed International |
| Distribution | US |
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 placement of 72 hours or less
Reason
Outer coating of the catheter may deteriorate and result in the coating to crack and/or potentially flake off
Identifiers
| code_info | Lot Numbers: 11247915, 11248510, 11248553, 11248938, 11248985, 11249049 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1276-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.