MAUDE Adverse Event Report: ASCENSIA DIABETES CARE US INC. CONTOUR NEXT; BLOOD GLUCOSE TEST STRIPS

Model Number	7313
Medical Device Problem Code	High Readings (2459)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	01/19/2019
Type of Reportable Event	Malfunction
Event or Problem Description
At 1:37 p.M., the customer obtained a blood glucose reading of 187 mg/dl on a contour next one meter.At 1:38 p.M., upon repeat testing, a reading of 97 mg/dl was obtained on a different meter.There was no allegation of adverse event.The customer was advised to return the test strips for evaluation.A replacement meter was sent to the customer.
Additional Manufacturer Narrative
The customer did not return the suspected product.The in-house contour next one meter was tested with the in-house contour next test strips from lot # 8epeb51a, which gave satisfactory performance.

• Brand Name: CONTOUR NEXT
• Common Device Name: BLOOD GLUCOSE TEST STRIPS
• Manufacturer (Section D): ASCENSIA DIABETES CARE US INC.; 100 summit lake drive; valhalla NY 10595
• MDR Report Key: 8324901
• Report Number: 1810909-2019-00073
• Device Sequence Number: 1717574
• Product Code: NBW
• UDI-Device Identifier: 10301937313100
• UDI-Public: 10301937313100
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K160682
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Other
• Remedial Action: Replace
• Type of Report: Initial,Followup
• Report Date (Section B): 01/19/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 05/31/2020
• Device Model Number: 7313
• Device Catalogue Number: 7313
• Device Lot Number: 8EPEB51A
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/19/2019
• Supplement Date Received by Manufacturer: 05/16/2019
• Initial Report FDA Received Date: 02/11/2019
• Supplement Report FDA Received Date: 06/14/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 55 YR