[Recalled] Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2) — Defective foam or an assembly error may cause the receiver speaker to lose cont… | FDA 2
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2) |
|---|---|
| Brand / manufacturer | Dexcom, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1945-2025 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 12 May 2025 |
| EAN / barcode | 00386270003812 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States 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
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
Related recalls from Dexcom, Inc.
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.