Finger Sensor for Remmers Recorder — Class II medical device recall Z-1725-2013
Terminated recall by SagaTech Electronics, Inc., reported 2013-07-17, distributed nationwide. The outer jacket is receding away from the black sensor prematurely.
| Recall number | Z-1725-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SagaTech Electronics, Inc., Calgary, Alberta, Canada |
| Recall initiated | 2008-05-08 |
| Classified | 2013-07-11 |
| Reported by FDA | 2013-07-17 |
| Terminated | 2013-07-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Lot numbers | 13367, 13710 |
| Model numbers | 1.1 |
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 for recall
The outer jacket is receding away from the black sensor prematurely.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1725-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.