Device recall
Z-0930-2021: B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a…
FDA device recall · Class II · Braxton Medical Corporation
Key facts
| Recall number (Z-number) | Z-0930-2021 |
|---|---|
| Recall event | 86443 |
| Product | B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular. |
| Product code | FOZ |
| Recalling firm | Braxton Medical Corporation |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003499504 |
At a glance
- None 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