Device recall
Z-0873-2022: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems…
FDA device recall · Class II · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-0873-2022 |
|---|---|
| Recall event | 89784 |
| Product | Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (END) - VERSION 2, Article Code Number 3456103A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI 04046964285608)… |
| Product code | KDI |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2024 |
| 510(k) numbers | K083460 |
| FEI number | 2521402 |
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