FDA Adverse Event Malfunction Summary report: N

OMNIPOD 5 PODS

MDR report key: 22014127 · Received May 13, 2025

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

Additional Manufacturer Narrative · 0

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.

Description of Event or Problem · 0

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