FDA Adverse Event Malfunction Summary report: N

FREESTYLE FLASH

MDR report key: 3665728 · Received March 6, 2014

Report

Report Number
2954323-2014-00204
Event Type
Malfunction
Date Received
March 6, 2014
Date of Event
January 8, 2014
Report Date
February 6, 2014
Product Code
LFR
PMA / PMN Number
K092638
Removal / Correction Number
ADC FA1002-2014
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE FREESTYLE TEST STRIP LOT THAT IS REFERENCED IN THIS MDR IS ASSOCIATED WITH AN ON-GOING RECALL. THE FDA WAS INFORMED OF THE FIELD ACTION PER 21CFR806 (RECALL NUMBER 2954323-02/07/14-001-R) AND AFFECTED CONSIGNEES WERE NOTIFIED BY LETTER BEGINNING FEBRUARY 19, 2014. ADC HAS IDENTIFIED THAT ALL NON-APPLIED VOLTAGE LEGACY BLOOD GLUCOSE METERS (0MV) MAY PRODUCE ERRONEOUSLY LOW BLOOD GLUCOSE READINGS IN THE PARKES ERROR GRID C OR D ZONE THAT COULD POTENTIALLY AFFECT CLINICAL OUTCOME WHEN USED IN CONJUNCTION WITH FREESTYLE TEST STRIP LOT WITHIN EXPIRY. THIS ISSUE ONLY OCCURS WHEN FREESTYLE OR FREESTYLE LITE BLOOD GLUCOSE TEST STRIPS ARE USED WITH FREESTYLE, FREESTYLE FLASH BLOOD GLUCOSE METERS AND THE FREESTYLE BLOOD GLUCOSE METER BUILT INTO THE OMNIPOD INSULIN MANAGEMENT SYSTEM AND FREESTYLE NAVIGATOR. NOTE: THE TEST STRIP LOT NUMBER IS UNKNOWN; THEREFORE, THE DEVICE MANUFACTURER DATE IS UNKNOWN. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT DIABETES CARE HAS BEEN SUBMITTED.

Description of Event or Problem · 1

INFORMATION WAS RECEIVED FROM THE OMNIPOD SYSTEM MANUFACTURER INSULET CORPORATION THAT WAS REPORTED UNDER MFR REPORT #3004464228-2014-0142. IT WAS REPORTED THE CUSTOMER'S OMNIPOD SYSTEM WAS READING LOWER THAN A HOSPITAL METER READING. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
137180 FREESTYLE FLASH BLOOD GLUCOSE MONITORING SYSTEM LFR UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 18 YR