Device recall
Z-0174-2023: BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1…
FDA device recall · Class II · Becton Dickinson Infusion Therapy Systems Inc.
Key facts
| Recall number (Z-number) | Z-0174-2023 |
|---|---|
| Recall event | 90972 |
| Product | BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr) |
| Product code | FOZ |
| Recalling firm | Becton Dickinson Infusion Therapy Systems Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183399 |
| FEI number | 1710034 |
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