Dexcom G6 Glucose Receivers Recalled for Delayed Alarms and Reading Errors

What You Should Do

1. The recalled products are Dexcom G6 Continuous Glucose Monitoring System touchscreen receivers with model references STK-OM-001, STR-OM-001, STR-OR-001, STK-OR-001, and STK-OE-001.
2. Check the back of your glucose receiver or the product packaging for model references (REF) STK-OM-001, STR-OM-001, STR-OR-001, STK-OR-001, or STK-OE-001. See the Affected Products section below for the full list of affected codes.
3. Stop using the recalled receiver and use an alternative method for glucose monitoring as directed by your healthcare professional.
4. Return the product to the place of purchase for a refund or replacement, throw it away, or contact Dexcom, Inc. or your medical distributor for instructions on how to receive a replacement or corrective update.
5. If you have health concerns or have experienced symptoms of high or low blood sugar while using the device, contact your healthcare provider immediately.
6. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) with any additional questions regarding this recall.

Your Remedy Options

You have 2 options:

Affected Products