MAUDE Adverse Event Report: ROCHE DIABETES CARE, INC. ACCU-CHEK ® COMPACT TEST DRUM; BLOOD GLUCOSE MONITORING TEST STRIPS

Model Number	05599415160
Medical Device Problem Code	Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	11/22/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Case with patient identifier (b)(6) is related to case with patient identifier (b)(6).
Event or Problem Description
It was reported the patient received the following results within 10 minutes: 148 mg/dl (aviva) and 300 mg/dl (compact).

• Brand Name: ACCU-CHEK ® COMPACT TEST DRUM
• Common Device Name: BLOOD GLUCOSE MONITORING TEST STRIPS
• Manufacturer (Section D): ROCHE DIABETES CARE, INC.; 9115 hague road; indianapolis IN 46250 0457
• MDR Report Key: 9489278
• Report Number: 3011393376-2019-04582
• Device Sequence Number: 10815247
• Product Code: NBW
• UDI-Device Identifier: 00075537474198
• UDI-Public: 00075537474198
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• PMA/510(K) Number: K031755
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/27/2020

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: 08/31/2019
• Device Model Number: 05599415160
• Device Catalogue Number: 05599415160
• Device Lot Number: 20816173
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 11/22/2019
• Supplement Date Received by Manufacturer: 04/14/2020
• Initial Report FDA Received Date: 12/18/2019
• Supplement Report FDA Received Date: 04/27/2020
• Patient Sequence Number: 1
• Patient Weight: 57