Device recall
Z-0306-2022: BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter…
FDA device recall · Class II · Becton Dickinson Infusion Therapy Systems Inc.
Key facts
| Recall number (Z-number) | Z-0306-2022 |
|---|---|
| Recall event | 88762 |
| Product | BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660 mL/hr)-0.5mL, REF 383536; BD Q-Style Luer Access Split Septum BD Vialon Material; BD Instaflash Needle Technology; Rx Only, Sterile EO. BD Nexiva closed IV catheter systems are… |
| 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