OMNIPOD 5 PODS
Report
- Report Number
- 3004464228-2025-20916
- Event Type
- Malfunction
- Date Received
- May 13, 2025
- Date of Event
- March 31, 2025
- Report Date
- May 13, 2025
- Manufacturer
- INSULET CORPORATION
- Product Code
- QFG
- UDI-DI
- 20385083000579
- 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. IT WAS REPORTED THAT THE CANNULA HAD DISLODGED FROM THE INFUSION SITE. THIS CONDITION COULD INTERRUPT INSULIN DELIVERY AND CONTRIBUTE TO HYPERGLYCEMIA. LOT RELEASE RECORDS WERE REVIEWED, AND THE PRODUCT LOT MET ALL ACCEPTANCE CRITERIA. SPECIFICALLY, A POD IS PAIRED TO A PDM AND PUT THROUGH SIMULATED USE TESTING INCLUDING COMMUNICATING WITH THE PDM, DEPLOYMENT, DELIVERING FLUID, OCCLUSION DETECTION, AND FREEDOM FROM HAZARD ALARMS. LOCKED DOWN SMARTPHONE: PHONE_CONTROL_ANDROID OMNIPOD SOFTWARE APP VERSION: 3.1.1 SMARTPHONE OPERATING SYSTEM: TP1A.220624. 014.G981U1UESCHXL1 SMARTPHONE HARDWARE: SM-G981U1 CGM SENSOR TYPE: G7. PLEASE NOTE, THAT SECTION D IS CAPTURING THE DEVICE IDENTIFIERS AS REPORTED BY THE COMPLAINANT. THIS MAY NOT ALIGN TO THE DEVICE CONFIGURATION REPORTED IN H11, AS THIS DATA IS PULLED FROM OUR CLOUD BASED ON THE REPORTED DATE OF EVENT.
IT WAS REPORTED THE PATIENT'S BLOOD GLUCOSE LEVEL (BG) ROSE TO OVER 250 MG/DL WHILE WEARING THE POD BETWEEN 4 AND 24 HOURS. WHILE THE PATIENT WAS WORKING AT THEIR COMPUTER, THE POD REPORTEDLY FELL OFF THE INFUSION SITE (ABDOMEN), CAUSING THE CANNULA TO DISLODGE. AS TREATMENT, THE PATIENT APPLIED A NEW POD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 879981 | OMNIPOD 5 PODS | OMNIPOD 5 PODS | QFG | INSULET CORPORATION | PT-001662 | PH1U08062432 | 20385083000579 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR | Male |