Device recall
Z-0121-2026: PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle…
FDA device recall · Class II · B BRAUN MEDICAL INC
Key facts
| Recall number (Z-number) | Z-0121-2026 |
|---|---|
| Recall event | 97550 |
| Product | PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle - 17 Ga. x 3-1/2 in. (8.9 cm) - Winged, PERIFIX FX Springwound Epidural Catheter - 19 Ga. Closed tip. Product Code: CE17TFC. Product Description: CE17TFC CONTINUOUS EPID SET W/17G TUOHY. |
| Product code | OGE |
| Recalling firm | B BRAUN MEDICAL INC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3013764800 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 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