Device recall
Z-0063-2017: Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end…
FDA device recall · Class II · A & D Enginering Inc
Key facts
| Recall number (Z-number) | Z-0063-2017 |
|---|---|
| Recall event | 75177 |
| Product | Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end users who are eighteen (18) years and older at home to monitor their blood pressure (systolic and diastolic) and pulse rate. |
| Product code | DXN |
| Recalling firm | A & D Enginering Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 28, 2018 |
| 510(k) numbers | K043217 |
| FEI number | 2082313 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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