FDA Adverse Event Malfunction Summary report: N

OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM

MDR report key: 23291237 · Received October 15, 2025

Report

Report Number
3004464228-2025-47997
Event Type
Malfunction
Date Received
October 15, 2025
Date of Event
September 27, 2025
Report Date
October 14, 2025
Manufacturer
INSULET CORPORATION
Product Code
QFG
UDI-DI
20385083000548
PMA / PMN Number
K231826
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

ACCORDING TO THE COMPLAINANT THE DEVICE WILL NOT BE RETURNED FOR INVESTIGATION. LOT RELEASE RECORDS WERE REVIEWED, AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA. WE ARE UNABLE TO CONFIRM OR DETERMINE THE ROOT CAUSE OF THE REPORTED DISLODGED CANNULA. LOCKED DOWN SMARTPHONE: LOCKDOWN. OMNIPOD SOFTWARE APP VERSION: 3.1.5-P001. OPERATING SYSTEM: N5004L-AM-Q-MV01602-06-01.06. HARDWARE: N5004L. CGM SENSOR TYPE: G6. PLEASE NOTE, THE DEVICE IDENTIFIERS ARE CAPTURED AS REPORTED BY THE COMPLAINANT AND MAY NOT ALIGN WITH THE DEVICE CONFIGURATION REPORTED IN THIS SECTION AS THIS DATA IS PULLED FROM OUR CLOUD BASED ON THE REPORTED DATE OF EVENT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE PATIENT'S BLOOD GLUCOSE LEVEL (BG) ROSE ABOVE 250 MG/DL WHILE WEARING THE POD BETWEEN 5 AND 24 HOURS. WHEN THE POD WAS REMOVED FROM THE INFUSION SITE (LEG), IT WAS OBSERVED THAT THE POD'S CANNULA WAS DISLODGED. THE PATIENT WAS PLAYING IN A PLAYGROUND WHEN THE DISLODGED CANNULA WAS OBSERVED. ADDITIONALLY, IT WAS REPORTED THAT THE POD WAS LEAKING INSULIN. AS TREATMENT A NEW POD WAS APPLIED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2415299 OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM AUTOMATED INSULIN DELIVERY SYSTEM QFG INSULET CORPORATION PT-001446 PH1K02092531 20385083000548

Patients

Seq Age Sex Outcome Treatment
1 15 YR Male