OMNIPOD INSULIN PUMP
Report
- Report Number
- 3004464228-2008-00188
- Event Type
- Malfunction
- Date Received
- August 29, 2008
- Date of Event
- June 14, 2008
- Report Date
- July 30, 2008
- Manufacturer
- INSULET CORPORATION
- Product Code
- LZG
- PMA / PMN Number
- K042792
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- NOT APPLICABLE
Narratives
THE PRODUCT WAS RETURNED AND EVALUATED. THE EVALUATION INDICATES A PROBABLE PROBLEM WITH THE RETAINER THAT ALLOWED A COMPONENT TO MOVE RESULTING IN DAMAGE. THIS DAMAGE PREVENTED THE PLUNGER FROM ADVANCING. THE USER WOULD HAVE BEEN AWARE OF A PROBLEM DURING THE FILL PROCESS. THERE IS RESISTANCE FELT IN FILLING THE POD WITH INSULIN AND A DISTINCT "CRACKLING" NOISE RESULTING FROM STRIPPING THE THREADS OF THE COMPONENT WHEN OVER-PRESSURIZED. THE OMNIPOD USER GUIDE STATES: "WARNING: NEVER USE A POD IF, DURING FILL, YOU DETECT ANY CRACKLING NOISE OR RESISTANCE WHILE DEPRESSING THE PLUNGER OF THE FILL SYRINGE. USING A POD WITH THESE CONDITIONS COULD RESULT IN UNDER-DELIVERY OF INSULIN." THE USER IS ALSO INSTRUCTED IN THE USER GUIDE TO MONITOR BLOOD GLUCOSE LEVELS FREQUENTLY. BY FOLLOWING THESE RECOMMENDATIONS, THE USER BECAME AWARE OF THEIR HIGH BLOOD GLUCOSE AND STARTED A NEW POD OR BACKUP THERAPY IF NEEDED.
CUSTOMER CALLED TO REPORT HIGH BLOOD GLUCOSE (BGS) AND UNSURE IF THIS POD IS WORKING PROPERLY. CUSTOMER STATED SHE HAS GIVEN A TOTAL OF 16 UNITS OF BOLUS INSULIN AND BG KEEPS CLIMBING (RANGED 289 - 491 MGD/DL). CUSTOMER TREATED HIGH BG WITH INSULIN PEN PRIOR TO ACTIVATING A NEW POD. CUSTOMER ABLE TO ACTIVATE A NEW POD AND WILL MONITOR BG CLOSELY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | OMNIPOD INSULIN PUMP | PUMP, INFUSION, INSULIN | LZG | INSULET CORPORATION | 11200 | L11708 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |