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Dexcom, Inc. recalls

The FDA has posted 18 enforcement recalls from Dexcom, Inc. since 2025, including 10 Class I (most serious) recalls. Most recent report: Jul 1, 2026.

Class I: 10Class II: 8
Class IOngoingZ-1945-2025

Dexcom, Inc. recalls Dexcom One+ Continuous Glucose Monitoring System

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.…

  • Factory Calibrated Integrated Continuous Glucose Monitoring System
  • Nonconforming Material/Component
Dexcom, Inc.CAJun 25, 2025
Class IOngoingZ-1946-2025

Dexcom, Inc. recalls Dexcom One Continuous Glucose Monitoring System

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.…

  • Factory Calibrated Integrated Continuous Glucose Monitoring System
  • Nonconforming Material/Component
Dexcom, Inc.CAJun 25, 2025

Firm name as filed with the FDA: “Dexcom, Inc.”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.