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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INSULET CORPORATION OMNIPOD DASH, PDM, PERSONAL DIABETES MANAGER; PUMP, INFUSION, INSULIN

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INSULET CORPORATION OMNIPOD DASH, PDM, PERSONAL DIABETES MANAGER; PUMP, INFUSION, INSULIN Back to Search Results
Model Number PT-000030
Device Problems Fluid/Blood Leak (1250); Material Rupture (1546)
Patient Problem Chemical Exposure (2570)
Event Date 11/23/2022
Event Type  malfunction  
Manufacturer Narrative
A technical assessment of the device design identified the root cause of the thermal event to be the dash pdm charging voltage exceeding the battery specification, defined as overcharging.Field safety corrective action has been initiated by insulet corporation.
 
Event Description
It was reported battery fluid was leaking from the personal diabetes manager (pdm) battery.The patient reported the battery life drained quickly.
 
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Brand Name
OMNIPOD DASH, PDM, PERSONAL DIABETES MANAGER
Type of Device
PUMP, INFUSION, INSULIN
Manufacturer (Section D)
INSULET CORPORATION
100 nagog park
acton MA 01720
Manufacturer (Section G)
INSULET CORPORATION
100 nagog park
acton MA 01720
Manufacturer Contact
michael spears
100 nagog park
acton, MA 01720
9786007000
MDR Report Key15970036
MDR Text Key306641681
Report Number3004464228-2022-23604
Device Sequence Number1
Product Code LZG
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K192659
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Consumer
Reporter Occupation Other
Type of Report Initial
Report Date 11/23/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/13/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberPT-000030
Device Catalogue NumberPDM-CAN-D001-MM
Was Device Available for Evaluation? No
Date Manufacturer Received11/23/2022
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Age22 YR
Patient SexFemale
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