🔍 RecallPedia

Finger Sensor for Remmers Recorder (Formerly SnoreSat Sleep recorder) To be used to gather heart rate and blood oxygen data during a sleep study.

Class I - Dangerous
🏥 Medical Devices Recalled: May 8, 2008 SagaTech Electronics Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model: 1.1 Lot numbers: 13367 and 13710
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
SagaTech Electronics, Inc.
Reason for Recall:
The outer jacket is receding away from the black sensor prematurely.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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 Codes/Lot Numbers:

Model: 1.1 Lot numbers: 13367 and 13710

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1725-2013