Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) SystemRecalls & reported problems across all models
Dexcom, Inc. · 6 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10,402
- Deaths reported
- 0
- Injuries reported
- 299
- Recalls
- 0
We found 6 models of Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System by Dexcom, Inc. in the FDA's device registry (GUDID). Together they are named in 10,402 adverse event reports in the FDA's MAUDE database, received between Sep 4, 2025 and Sep 30, 2026 — classified as 299 injuries, 10,093 malfunctions.
The most frequently reported specific device problem is “Wireless Communication Problem” (7,040 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System problems
Device problems
- Wireless Communication Problem7,040
- Low Readings1,734
- Detachment of Device or Device Component683
- High Readings411
- Break143
- Incorrect, Inadequate or Imprecise Result or Readings90
- Appropriate Device Problem Term/Code Not Available87
- Premature End-of-Life Indicator76
Patient problems
- No Clinical Signs, Symptoms or Conditions8,010
- Hyperglycemia1,729
- Hypoglycemia380
- Foreign Body In Patient183
- Loss of consciousness79
- Dizziness70
- Nausea70
- Malaise64
Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System STP-FT-012Integrated Continuous Glucose Monitoring System, Factory Calibrated5,305 reports
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System STP-FT-013Integrated Continuous Glucose Monitoring System, Factory Calibrated2,030 reports
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System STP-FT-010Integrated Continuous Glucose Monitoring System, Factory Calibrated1,527 reports
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System STE-FT-016Integrated Continuous Glucose Monitoring System, Factory Calibrated912 reports
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System STP-FT-011Integrated Continuous Glucose Monitoring System, Factory Calibrated627 reports
- Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System 9510Integrated Continuous Glucose Monitoring System, Factory Calibrated1 report
Recent Dexcom G7 15 Day Continuous Glucose Monitoring (CGM) System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50955178 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954987 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954986 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954982 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954980 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954968 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954851 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954846 ↗MalfunctionSep 30, 2026High Readings
Patient problems: Hypoglycemia
MAUDE report 50954772 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954752 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954742 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954740 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954737 ↗MalfunctionSep 30, 2026Low Readings
Patient problems: Hyperglycemia
MAUDE report 50954648 ↗MalfunctionSep 30, 2026Wireless Communication Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954618 ↗
Other Dexcom, Inc. products
- Dexcom G613 models · 637,302 reports · 7 recalls
- Dexcom G6 Transmitter2 models · 469,968 reports
- Dexcom G732 models · 325,909 reports · 8 recalls
- Dexcom G521 models · 206,314 reports · 1 recall
- Dexcom G7 GSS (161)4 models · 141,244 reports · 1 recall
- Dexcom G4 Platinum41 models · 119,308 reports · 2 recalls
- Dexcom G7 Receiver4 models · 33,732 reports · 1 recall
- Dexcom G7 GSS (160)4 models · 33,558 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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