FDA Adverse Event Malfunction Summary report: N

OT PING METER

MDR report key: 1934226 · Received December 21, 2010

Report

Report Number
2939301-2010-10895
Event Type
Malfunction
Date Received
December 21, 2010
Report Date
December 6, 2010
Manufacturer
LIFESCAN INC.
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

LIFESCAN (LFS) HAS REQUESTED RETURN OF THE SUBJECT PRODUCT(S) FOR EVALUATION. IF THE PRODUCT(S) ARE RETURNED, LFS WILL EVALUATE IT/THEM AND INFORM FDA OF PRODUCT(S) THAT DO NOT PASS INSPECTION IN A SUPPLEMENTAL REPORT. 510(K) # IS K080639.

Description of Event or Problem · 1

ON (B)(6) 2010 THE LAY USER/REPORTER, THE PATIENT'S MOTHER, CONTACTED LIFESCAN TO REPORT THE ONE TOUCH PING METER OK BUTTON WAS INTERMITTENTLY UNRESPONSIVE. THE SR. MEDICAL SURVEILLANCE SPECIALIST WAS ABLE TO CLASSIFY THE COMPLAINT BASED ON THE INFORMATION ORIGINALLY PROVIDED. ON APPROXIMATELY (B)(6) 2010 THE PATIENT NOTED THE UP OK BUTTON ON THE REPORTED METER WAS INTERMITTENTLY NOT RESPONDING. AT THAT SAME TIME, THE PATIENT WAS EXPERIENCING THE SYMPTOMS OF HEADACHE, THIRST AND IMPAIRED VISION. THE PATIENT ADMINISTERED SELF-TREATMENT BY TAKING FIVE UNITS NOVOLOG INSULIN USING HER PUMP; SHE DID NOT SEEK ANY MEDICAL ATTENTION. TROUBLESHOOTING REVEALED THIS WAS NOT A NEW METER AND THERE HAD BEEN NO MISUSE OF THE PRODUCT. THE ISSUE WAS NOT RESOLVED. THE METER WAS REPLACED. THE PATIENT DID NOT SUFFER AN ADVERSE EVENT DUE TO THE REPORTED METER. THE PATIENT'S SYMPTOMS WERE NOT INDICATIVE OF SEVERE INJURY AND BEGAN PRIOR TO THE METER ISSUE, THERE WAS NO DELAY IN TREATMENT, AND THE PATIENT DENIED SEEKING MEDICAL ATTENTION. HOWEVER, AS THE METER ISSUE WAS NOT RESOLVED, THIS COMPLAINT IS BEING REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OT PING METER GLUCOSE MONITORING SYS/KIT NBW LIFESCAN INC. 2934274

Patients

Seq Age Sex Outcome Treatment
1 13 YR