PRECISION XTRA
Report
- Report Number
- 2954323-2011-01526
- Event Type
- Malfunction
- Date Received
- February 8, 2011
- Date of Event
- January 6, 2011
- Report Date
- February 8, 2011
- Product Code
- NBW
- Removal / Correction Number
- ADC FA1197-2010
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
Narratives
RETAIN SAMPLES OF PRECISION TEST STRIP LOTS MANUFACTURED WITH HOT-MELT GLUE BATCHES EXHIBITED LOWER THAN EXPECTED READINGS ON CONTINUOUS STORAGE AFTER NINE MONTHS AT 30 DEGREES CELSIUS DURING ROUTINE STABILITY PERFORMANCE TESTING. THIS STABILITY ISSUE COULD LEAD TO THE GENERATION OF INCORRECTLY DEPRESSED BLOOD GLUCOSE RESULTS AND THESE ERRONEOUS RESULTS MAY BE IN THE "C", "D" OR "E" ZONES OF PARKES ERROR GRID, AND AS SUCH, HAVE THE POTENTIAL TO BE CLINICALLY SIGNIFICANT. THE PRIMARY CAUSE HAS BEEN IDENTIFIED TO BE BATCH TO BATCH GLUE VARIABILITY. THE FDA HAS BEEN INFORMED OF THE FIELD ACTION ((B)(4)). (B)(4).
CUSTOMER REPORTED RECEIVING THE FOLLOWING RESULTS FROM HER PRECISION XTRA BLOOD GLUCOSE METER, WHICH WERE LOWER THAN SHE FELT: 96 MG/DL ON (B)(6) 2011, 97 MG/DL ON (B)(6) 2011 AND 88 MG/DL ON (B)(6) 2011. ALL RESULTS WERE OBTAINED BEFORE BREAKFAST. SHE FURTHER REPORTED EXPERIENCING DIAPHORESIS AND VERTIGO. NO THIRD-PARTY EMERGENT INTERVENTION WAS REPORTED. CUSTOMER SELF-TREATED WITH CANDY AND JUICE. IT WAS ADDITIONALLY REPORTED THE CUSTOMER HAD BEEN USING TEST STRIPS RELATED TO AN ON-GOING FIELD ACTION FOR ABBOTT'S PRECISION FAMILY TEST STRIPS. THERE WAS NO REPORT OF DEATH OR PERMANENT INJURY ASSOCIATED WITH THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRECISION XTRA | BLOOD GLUCOSE MONITORING SYSTEM | NBW | 45001A918 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |