MAUDE Adverse Event Report: INSULET CORPORATION OMNIPOD 5 PODS

Model Number	PT-001662
Medical Device Problem Codes	Loss of or Failure to Bond (1068); Unintended Movement (3026)
Health Effect - Clinical Code	Hyperglycemia (1905)
Date of Event	12/31/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device has not been returned/received to date.If the device is received, a supplemental report will be submitted with the investigation results.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: phone_control_ios.Omnipod software app version: 2.1.0.Operating system: 26.1.Hardware: iphone 15.4.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.
Event or Problem Description
It was reported the patient's blood glucose level rose greater than 250 mg/dl while wearing the pod between 24 and 36 hours.The adhesive completely separated from the (arm) causing the cannula to dislodge.A new pod was successfully applied.

• Brand Name: OMNIPOD 5 PODS
• Common Device Name: OMNIPOD 5 PODS
• Manufacturer (Section D): INSULET CORPORATION; 100 nagog park; acton MA 01720
• Manufacturer (Section G): INSULET CORPORATION; 100 nagog park; acton MA 01720
• Manufacturer Contact: derek heyl ; 100 nagog park; acton, MA 01720 ; 9786007000
• MDR Report Key: 24147524
• Report Number: 3014585508-2026-03154
• Device Sequence Number: 8705878
• Product Code: QFG
• UDI-Device Identifier: 20385083000579
• UDI-Public: (01)20385083000579(11)250702(17)270702(10)PH1U07022521
• Combination Product (Y/N): N
• PMA/510(K) Number: K231826
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 01/22/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: PT-001662
• Device Catalogue Number: POD-OMNI-I1-6720
• Device Lot Number: PH1U07022521
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 12/31/2025
• Initial Report FDA Received Date: 01/22/2026
• Date Device Manufactured: 07/02/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Age: 23 YR
• Patient Sex: Female