OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM
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
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.
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 |