FDA Adverse Event Injury Summary report: N

DEXCOM G7 CGM

MDR report key: 25140595 · Received May 11, 2026

Report

Report Number
MW5187945
Event Type
Injury
Date Received
May 11, 2026
Date of Event
March 14, 2026
Report Date
May 7, 2026
Manufacturer
DEXCOM, INC.
Product Code
QBJ
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

I AM HAVING A BAD SKIN REACTION TO THE DEXCOM G7 CONTINUOUS GLUCOSE MONITORING. I HAVE GIANT PATCHES ON BOTH ARMS THAT ARE PAINFUL, ITCHY, AND SPREADING. THEY LIKELY CHANGED THEIR ADHESIVE WHEN THEY TRIED TO GET 15 DAY APPROVAL. I'M IN A LOT OF PAIN AND HAVE TRIED STEROID CREAMS BUT THE AREAS ARE NOT IMPROVING. I RELY ON THE CONTINUOUS GLUCOSE MONITORING AND DON'T HAVE ANY OPTION BUT TO KEEP USING IT DESPITE THE VERY UNCOMFORTABLE PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
519349 DEXCOM G7 CGM INTEGRATED CONTINUOUS GLUCOSE MONITORING SYSTEM, FACTORY CALIBRATED QBJ DEXCOM, INC.

Patients

Seq Age Sex Outcome Treatment
1 36 YR Female