FDA Adverse Event Malfunction Summary report: N

OT PING METER

MDR report key: 1880753 · Received October 25, 2010

Report

Report Number
2939301-2010-09369
Event Type
Malfunction
Date Received
October 25, 2010
Report Date
October 18, 2010
Manufacturer
LIFESCAN INC.
Product Code
NBW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE LAY USER/PATIENT'S METER HAS BEEN RETURNED AND EVALUATED BY LIFESCAN PRODUCT ANALYSIS WITH THE FOLLOWING FINDINGS: THE METER INVOLVED IN THIS CASE HAS PASSED TESTING WITH NO FAULTS FOUND. IF ANY ADDITIONAL INFORMATION IS AVAILABLE, THE FDA WILL BE NOTIFIED IN A SECOND FOLLOW UP REPORT. AT THIS TIME, WE CONSIDER THIS MATTER CLOSED.

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 K082590.

Description of Event or Problem · 1

SUBSEQUENT TO THE INITIAL MEDWATCH ADDITIONAL INFORMATION WAS RECEIVED REPORTING THAT THE PROMUS STENT DELIVERY SYSTEM WAS NEVER INSIDE THE PATIENT BECAUSE THE DEVICE BECAME STUCK ON THE GUIDE WIRE DURING ADVANCEMENT. DURING ATTEMPTS TO PULL THE DEVICE BACK, THE DISTAL SHAFT SEPARATED AND THE STENT DISLODGED. THE PATIENT'S CURRENT CONDITION IS EXCELLENT.

Description of Event or Problem · 1

THE LAY USER/PATIENT CONTACTED LIFESCAN ALLEGING THE METER POWERS OFF DURING USE. THE ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WERE NO ALLEGATIONS OF HARM OR INJURY. REPLACEMENT PRODUCTS WERE SENT TO THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OT PING METER GLUCOSE MONITORING SYS/KIT NBW LIFESCAN INC. 3032378

Patients

Seq Age Sex Outcome Treatment
1