Device recall
Z-0633-2014: The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN…
FDA device recall · Class II · Welch Allyn Protocol, Inc
Key facts
| Recall number (Z-number) | Z-0633-2014 |
|---|---|
| Recall event | 66919 |
| Product | The Propaq LT Series monitors. Model numbers 802LTAN, 802LT0N, and 802LTRN. These devices are indicated for ECG, noninvasive blood pressure (NIBP), respiration and SpO2. The most likely locations for patients to be monitored by these devices are hospital general medical-surgical, telemetry, and… |
| Product code | MWI |
| Recalling firm | Welch Allyn Protocol, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2015 |
| 510(k) numbers | K033378 |
| FEI number | 3023750 |
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