Device recall
Z-1777-2017: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY…
FDA device recall · Class II · Welch Allyn Inc
Key facts
| Recall number (Z-number) | Z-1777-2017 |
|---|---|
| Recall event | 76552 |
| Product | Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C. --- Microlife AG Espenstrasse… |
| Product code | DXN |
| Recalling firm | Welch Allyn Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 14, 2019 |
| 510(k) numbers | K152770 |
| FEI number | 1316463 |
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