FDA Adverse Event Injury Summary report: N

CEQUR SIMPLICITY

MDR report key: 24746481 · Received March 31, 2026

Report

Report Number
3015218509-2026-00001
Event Type
Injury
Date Received
March 31, 2026
Date of Event
March 2, 2026
Report Date
March 31, 2026
Manufacturer
CEQUR SA
Product Code
OPP
UDI-DI
00373108000006
PMA / PMN Number
K233447
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

A PATIENT NOTIFIED A CEQUR EMPLOYEE ON 02MAR2026 THAT WHILE WEARING A CEQUR SIMPLICITY DEVICE, SHE EXPERIENCED HYPOGLYCEMIA. THE PATIENT REPORTED THAT AFTER APPLYING A NEW DEVICE IN THE EVENING ON (B)(6) 2026, AROUND 3:00 AM THE NEXT MORNING, HER CONTINUOUS GLUCOSE MONITOR DISPLAYED GLUCOSE LEVELS BETWEEN 47 AND 52 MG/DL. THE PATIENT CONSUMED SIX CRACKERS, AND HER GLUCOSE LEVELS ROSE, BUT THE CONTINUOUS GLUCOSE MONITOR'S ALARM CONTINUED TO WAKE HER UP THROUGH THE REST OF THE MORNING. THE PATIENT REPORTED THAT HER GLUCOSE LEVEL WAS 67 MG/DL BEFORE BREAKFAST AND THAT SHE ADMINISTERED FOUR UNITS OF INSULIN WITH BREAKFAST. HER CONTINUOUS GLUCOSE MONITOR'S ALARM SOUNDED AGAIN, SO SHE CONSUMED COTTON CANDY IN AN ATTEMPT TO RAISE HER GLUCOSE LEVELS. BEFORE LUNCH, HER GLUCOSE LEVEL WAS 72 MG/DL. SHE ATE BUT DID NOT DOSE INSULIN USING THE DEVICE. THE PATIENT STATED THAT HER GLUCOSE LEVELS WENT DOWN TO 52 MG/DL. SHE SUBSEQUENTLY REMOVED THE SIMPLICITY DEVICE AROUND 2:00 PM. WHEN SHE REMOVED THE DEVICE, SHE NOTICED THAT THE LOCATION WHERE THE PATCH WAS APPLIED WAS WET. SHE ALSO STATED THAT INSULIN "WAS DRIPPING FROM THE END OF THE CANNULA WITHOUT ANY BUTTONS BEING PRESSED." THE PATIENT APPLIED A NEW PATCH AND HER GLUCOSE LEVELS RETURNED TO NORMAL. THE PATIENT DID NOT SAVE THE CEQUR SIMPLICITY DEVICE BUT WAS ABLE TO PROVIDE THE LOT NUMBER. AN INVESTIGATION OF THE LOT DEVICE HISTORY RECORD REVEALED NO NONCONFORMITIES OR DEVIATION RELATED TO THE NATURE OF THE COMPLAINT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
800811 CEQUR SIMPLICITY Pump, infusion, insulin bolus OPP CEQUR SA CQR-S-2U0 FT2504991 00373108000006

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention