FDA Adverse Event Injury Summary report: N

OMNIPOD INSULIN PUMP

MDR report key: 1911791 · Received November 24, 2010

Report

Report Number
3004464228-2010-01393
Event Type
Injury
Date Received
November 24, 2010
Date of Event
October 27, 2010
Report Date
October 27, 2010
Manufacturer
INSULET CORPORATION
Product Code
LZG
PMA / PMN Number
K042792
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE POD WILL NOT BE RETURNED FOR EVALUATION. UNABLE TO CONFIRM ANY ISSUE RELATED TO THE POD'S ADHESIVE THAT MAY HAVE RESULTED IN THE CUSTOMER'S ADVERSE SKIN CONDITION. THE OMNIPOD USER GUIDE INSTRUCTS PTS TO CHECK THE INFUSION SITE DAILY FOR SINGS OF INFECTION SUCH AS PAIN, SWELLING, REDNESS, DISCHARGE OR HEAT. IF THERE ARE SIGNS THAT THE SITE MAY BE INFECTED, THE PT IS ADVISED TO IMMEDIATELY REMOVE THE POD AND APPLY A NEW ONE, CONTACT A HEALTH CARE PROVIDER AND TREAT THE INFECTION ACCORDING TO THE HEALTH CARE PROVIDER'S INSTRUCTIONS. THE CUSTOMER FOLLOWED THESE INSTRUCTIONS PER THE USER GUIDE AND WAS PLACED ON ANTIBIOTICS AT THE RECOMMENDATION OF HER DOCTOR IN ORDER TO TREAT THE ABSCESS. THE OMNIPOD WEBSITE OFFERS A RESOURCE GUIDE THAT INCLUDES A LISTING OF SKIN BARRIER PRODUCTS THAT CAN AID IN SKIN PROTECTION.

Description of Event or Problem · 1

THE REPORT INDICATED THAT THE CUSTOMER EXPERIENCED A SKIN ABSCESS FROM WEARING THE POD. AS A RESULT, SHE WAS PLACE ON ANTIBIOTICS BY HER DOCTOR. INSULET CUSTOMER CARE REVIEWED PROPER POD PLACEMENT AND SKIN PREPARATION TECHNIQUE WITH THE CUSTOMER. A FOLLOW-UP PLAN WAS MADE TO CHECK BACK WITH THE CUSTOMER IN ONE MONTH'S TIME. NO PRODUCT WILL BE RETURNED FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OMNIPOD INSULIN PUMP PUMP, INFUSION, INSULIN LZG INSULET CORPORATION 11200 UNAVAILABLE

Patients

Seq Age Sex Outcome Treatment
1 60 YR Other