Device recall
Z-0110-2015: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are…
FDA device recall · Class II · Mortara Instrument, Inc
Key facts
| Recall number (Z-number) | Z-0110-2015 |
|---|---|
| Recall event | 69467 |
| Product | Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage: They are indicated for use in adult & pediatric patient populations. They facilitate the monitoring of: Non-invasive blood pressure (NIBP), Impedance respiration, Invasive blood pressure (P1-P4), Temperature, Functional arterial… |
| Product code | MHX |
| Recalling firm | Mortara Instrument, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 13, 2015 |
| 510(k) numbers | K123556 |
| FEI number | 2183461 |
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