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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LIFESCAN EUROPE GMBH OT VERIO 2 METER; GLUCOSE MONITORING SYS/KIT

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LIFESCAN EUROPE GMBH OT VERIO 2 METER; GLUCOSE MONITORING SYS/KIT Back to Search Results
Model Number 022-657
Medical Device Problem Code Incorrect, Inadequate or Imprecise Result or Readings (1535)
Health Effect - Clinical Codes Fatigue (1849); Memory Loss/Impairment (1958); Dysphasia (2195); Confusion/ Disorientation (2553)
Date of Event 10/12/2020
Type of Reportable Event Serious Injury
Event or Problem Description
On (b)(6) 2020, the lay-user/patient contacted lifescan (lfs) (b)(4), alleging that her onetouch verio2 meter read inaccurately high compared to her feelings and/or normal readings.The complaint was classified based on the customer care agent (cca) documentation.The patient reported that on (b)(6) 2020 at 7:18 pm, she obtained what she felt was an inaccurate high blood glucose reading of "444 mg/dl" with the subject meter.The patient informed the cca that she manages her diabetes with oral medication (metformin 700 mg three times a day) and insulin (20 units novolog after lunch; 20-30 units of toujeo before bed based on food intake).When she obtained the elevated result, the patient claimed she took an extra dose of 20 units of novolog insulin.The patient claimed she retested her blood glucose with the subject meter and obtained results of "427, 371, 307 and 373 mg/dl" at 7:28 pm, 7:43 pm, 8:11 pm and 8:30 pm respectively.The patient stated that she began to develop symptoms of feeling "weak, no energy, lost memory, confusion and can't talk" at 8:30 pm.The patient claimed her daughter contacted the emergency room for assistance and was instructed to take her to hospital.However, the patient stated she consumed food as self-treatment for the symptoms; symptoms which lasted 1 hour.She claimed she felt better after treatment and slept until 6:30 am the next day.Prior to when the alleged issue occurred, the patient claimed she tested her blood glucose with the subject meter on (b)(6) 2020 at 3:51 pm and obtained a result of "84 mg/dl." the patient stated she thought she could last until the evening meal but since she was carrying out physical work, she started "shaking" after the physical effort.She took 10 g of grapes and a juice as self-treatment for the symptom.At the time of troubleshooting, the cca confirmed that the unit of measure was set correctly on the subject meter.The cca noted the patient was testing with test strips that were stored correct and were not expired or opened past their discard date.Replacement products were sent to the patient.This complaint is being reported because the patient reportedly developed signs/symptoms suggestive of a serious injury adverse event after taking extra insulin based on an alleged inaccurate high result obtained with the subject meter.
 
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Brand Name
OT VERIO 2 METER
Common Device Name
GLUCOSE MONITORING SYS/KIT
Manufacturer (Section D)
LIFESCAN EUROPE GMBH
gubelstrasse 34
zug, 6300
SZ  6300
MDR Report Key10810160
Report Number2939301-2020-02754
Device Sequence Number11784474
Product Code NBW
UDI-Device Identifier00353885008716
UDI-Public00353885008716
Combination Product (Y/N)N
Initial Reporter CountryFR
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)Unknown
Reporter Type Importer
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 10/13/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Operator of Device Lay User/Patient
Device Model Number022-657
Device Catalogue Number022-657
Device Lot Number4655428
Was Device Available for Evaluation? No
Was the Report Sent to FDA? Yes
Distributor Facility Aware Date10/13/2020
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date11/09/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Outcome Attributed to Adverse Event Life Threatening; Required Intervention;
Patient Age56 YR
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