OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM
Report
- Report Number
- 3004464228-2025-51856
- Event Type
- Malfunction
- Date Received
- October 29, 2025
- Date of Event
- July 20, 2025
- Report Date
- November 24, 2025
- Manufacturer
- INSULET CORPORATION
- Product Code
- QFG
- UDI-DI
- 10385083000138
- PMA / PMN Number
- K203768
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
- Health Professional
- N
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: 3.1.2-P001. OPERATING SYSTEM: N5004L-AM-Q-MV01602-06-01.06. HARDWARE: N5004L. CGM SENSOR TYPE: G7. 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.
CORRECTED D4 - MODEL # TO PT-001446. CORRECTED D4 - CATALOG # TO POD-OMNI-I1-6720.
IT WAS REPORTED THE PATIENT'S BLOOD GLUCOSE LEVEL ROSE TO ABOVE 13.9 MMOL/L (>250 MG/DL) WHILE WEARING THE POD. THE POD REPORTEDLY WAS COMING LOOSE FROM THE INFUSION SITE (ARM), CAUSING THE CANNULA TO DISLODGE. AS TREATMENT, A NEW POD WAS PLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2686456 | OMNIPOD 5 AUTOMATED INSULIN DELIVERY SYSTEM | ALTERNATE CONTROLLER ENABLED INSULIN INFUSION PUMP | QFG | INSULET CORPORATION | PT-001446 | 10385083000138 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 46 YR | Female |