Device recall
Z-1276-2021: Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter…
FDA device recall · Class II · Epimed International, Inc.
Key facts
| Recall number (Z-number) | Z-1276-2021 |
|---|---|
| Recall event | 87333 |
| 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 |
| Product code | BSO |
| Recalling firm | Epimed International, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 17, 2022 |
| 510(k) numbers | K954584 |
| FEI number | 1316297 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database