Device recall
Z-1133-04: 18G Catheter is a component in various kits.
FDA device recall · Class II · Braun,B Medical Inc
Key facts
| Recall number (Z-number) | Z-1133-04 |
|---|---|
| Recall event | 28911 |
| Product | 18G Catheter is a component in various kits. |
| Product code | LJS |
| Recalling firm | Braun,B Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2004 |
| 510(k) numbers | K961745, K971085 |
| FEI number | 2523676 |
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