[Recalled] Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep study. — The outer jacket is receding away from the black sensor prematurely | FDA 2008
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| 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 / manufacturer | SagaTech Electronics, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1725-2013 |
| Country of notice | Canada |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 08 May 2008 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The outer jacket is receding away from the black sensor prematurely.
This Class II recall concerns device products distributed in Canada and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
- Top-Rated Cheese Brands You Need to Try in 2025
- Is E920 (L-Cysteine) Safe to Eat? What It Is and Why It's in Your Bread
- Best Vegan Products 2024: A Comprehensive Guide for Ethical & Sustainable Living
- Budget-Friendly Plant-Based Foods and Beverages: A Guide for Every Home
- Beauty Safety and Ingredients: What You Need to Know
- What is 1,2-dichloroethane (CAS 107-06-2)? Safety, Regulation & EU/US/Canada Perspective | ProductGuru