Device recall
Z-1725-2013: Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used…
FDA device recall · Class II · SagaTech Electronics, Inc.
Key facts
| Recall number (Z-number) | Z-1725-2013 |
|---|---|
| Recall event | 65148 |
| Product | Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep study. |
| Product code | MNR |
| Recalling firm | SagaTech Electronics, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 22, 2013 |
| 510(k) numbers | K002159 |
| FEI number | 3003081035 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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