Dexcom, Inc.: Device Recall
Recall #Z-1943-2025 · 05/12/2025
Recall Details
- Recall Number
- Z-1943-2025
- Classification
- Class I
- Product Type
- Device
- Recalling Firm
- Dexcom, Inc.
- Status
- Ongoing
- Date Initiated
- 05/12/2025
- Location
- San Diego, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 36,824 units
Reason for Recall
Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A missed audible alert for low or high blood glucose values could lead to untreated hypo or hyperglycemia which can cause seizures, vomiting, loss of consciousness, or death.
Product Description
Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
Distribution Pattern
worldwide distribution - US Nationwide and the countries of Andorra, Argentina Australia, Austria, Bahrain, Belgium, Bulgaria, Canada, Croatia, Czech Republic, Denmark, Estonia, Finland, France, Greece, Hong Kong, Ireland, Israel, Italy, Japan, Korea, Latvia, Liechtenstein, Lithuania, Luxembourg, Malta, Netherlands, New Zealand, Norway, Oman, Poland, Romania, Saudi Arabia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Turkey, United Kingdom.
Other Recalls by Dexcom, Inc.
- Class I: Dangerous 08/28/2025
- Class I: Dangerous 07/24/2025
- Class I: Dangerous 07/24/2025
- Class I: Dangerous 07/24/2025
- Class I: Dangerous 07/24/2025