MAUDE Adverse Event Report: ABBOTT DIABETES CARE INC. PRECISION XCEED PRO; BLOOD GLUCOSE MONITORING SYSTEM

Model Number	70900-01
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	09/01/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The product has been requested back for investigation.A follow- up report will be submitted once additional information is obtained.Note: the meter is designed to report readings between 20 mg/dl to 500 mg/dl.It should be noted that this meter does not give numeric value for readings less than 20 mg/dl or greater than 500 mg/dl.A "lo" display message indicates a reading less than 20 mg/dl and a "hi" display message indicates a reading greater than 500 mg/dl.The date entered is the date abbott diabetes care became aware of the event as the manufacture date is unknown.All pertinent information available to abbott diabetes care has been submitted.
Event or Problem Description
A hospital reported that a specific adc test strip lot was producing erratic readings across the hospital when used with different adc meters.It was reported that readings of <20 mg/dl and >500 mg/dl were received when using strip lot 4c785h when attempting to obtain patient results and that multiple tests were being performed (within 10 minutes) in order to get a valid test result.The reporter provided data documenting reading comparisons taken between (b)(6) 2017 through (b)(6) 2017.Multiple sets of readings when plotted on the parkes error grid fell into the ¿c¿ zone showing the difference in values to be clinically significant.There was no report of death, serious injury or mistreatment associated with this event.
Additional Manufacturer Narrative
The reported test strips were returned and investigated with a retained meter.The complaint was not confirmed and no new issues were observed.All results were within range specification and no errors were observed during control solution testing.This also serves as a correction report.(initial reported email address) was inadvertently omitted from the initial mdr 30 day report.
Event or Problem Description
A hospital reported that a specific adc test strip lot was producing erratic readings across the hospital when used with different adc meters.It was reported that readings of <20 mg/dl and >500 mg/dl were received when using strip lot 4c785h when attempting to obtain patient results and that multiple tests were being performed (within 10 minutes) in order to get a valid test result.The reporter provided data documenting reading comparisons taken between (b)(6) 2017 through (b)(6) 2017.Multiple sets of readings when plotted on the parkes error grid fell into the ¿c¿ zone showing the difference in values to be clinically significant.There was no report of death, serious injury or mistreatment associated with this event.

• Brand Name: PRECISION XCEED PRO
• Common Device Name: BLOOD GLUCOSE MONITORING SYSTEM
• Manufacturer (Section D): ABBOTT DIABETES CARE INC.; 1360 south loop road; alameda CA 94502 7001
• MDR Report Key: 7043454
• Report Number: 2954323-2017-08015
• Device Sequence Number: 2037225
• Product Code: NBW
• UDI-Device Identifier: 00093815709329
• UDI-Public: (01)00093815709329(17)20180831(10)4C785H
• Combination Product (Y/N): N
• Initial Reporter State: MI
• PMA/510(K) Number: K080960
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/05/2018

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: Health Professional
• Device Expiration Date: 08/31/2018
• Device Model Number: 70900-01
• Device Catalogue Number: 70932
• Device Lot Number: 4C785H
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/05/2018
• Initial Date Received by Manufacturer: 10/23/2017
• Supplement Date Received by Manufacturer: 01/08/2018
• Initial Report FDA Received Date: 11/17/2017
• Supplement Report FDA Received Date: 02/05/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1