FDA Device recall Z-1725-2013
Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep…
- FDA Device
- Class II
- terminated
- Published 2013-07-17
On 2013-07-17 the FDA classified a Class II recall of Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep… by Sagatech Electronics, citing the outer jacket is receding away from the black sensor prematurely.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1725-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2008-05-08 |
| Published | 2013-07-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sagatech Electronics |
| Distribution | US |
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.
Reason
The outer jacket is receding away from the black sensor prematurely.
Identifiers
| code_info | Model: 1.1 Lot numbers: 13367 and 13710 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1725-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.