Device recall
Z-1532-2016: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Product Code 710200K…
FDA device recall · Class I · B Braun Medical Inc
Key facts
| Recall number (Z-number) | Z-1532-2016 |
|---|---|
| Recall event | 73744 |
| Product | Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Product Code 710200K Serial # >202169 and < 203249 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health center and… |
| Product code | KDI |
| Recalling firm | B Braun Medical Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 11, 2017 |
| 510(k) numbers | K083460, K963440 |
| 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