SagaTech Electronics, Inc. Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep study. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
SagaTech Electronics, Inc.
Lot Codes / Batch Numbers
Model: 1.1 Lot numbers: 13367 and 13710
Products Sold
Model: 1.1 Lot numbers: 13367 and 13710
SagaTech Electronics, Inc. is recalling Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart ra due to The outer jacket is receding away from the black sensor prematurely.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The outer jacket is receding away from the black sensor prematurely.
Recommended Action
Per FDA guidance
SagaTech Electronics Inc, sent a letter to their Customers dated May 2008. The letter identified the product the problem and the action needed to be taken by the customer. Please take particular attention when cleaning these sensors by holding the cable somewhere in the middle and clean towards each end. This should become standard practice with all sensors to prolong their lifespan. If you have further questions please call (403) 228-4214 ext. 234.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026