Device recall
Z-0117-2026: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in…
FDA device recall · Class II · B BRAUN MEDICAL INC
Key facts
| Recall number (Z-number) | Z-0117-2026 |
|---|---|
| Recall event | 97550 |
| Product | PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Open tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKF. Product Description: CE17TKF PERIFIX CONTIN. EPIDURAL TRAY |
| 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