MAUDE Adverse Event Report: LIFESCAN INC ONETOUCH ULTRA2; GLUCOSE MONITORING SYS/KIT

Model Number	024-046
Medical Device Problem Code	Device Displays Incorrect Message (2591)
Health Effect - Clinical Code	Malaise (2359)
Date of Event	03/21/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
On (b)(6) 2025, the lay user/patient contacted lifescan (lfs) united states, alleging that his onetouch ultra2 meter displayed error messages ¿error 2, error 4 and error 5¿ during testing.The complaint was classified based on the customer care agent (cca) documentation, since the patient was unable to be reached by phone for additional information.The patient reported that since he got the meter on (b)(6) 2025, he had been unable to test his blood glucose due to the error messages appearing.It was not reported if the patient takes any medication to manage his diabetes or if he made any changes to his usual diabetes management regimen.As a result of the alleged issue, the patient mentioned that on (b)(6) 2025, he went to the hospital because he was ¿feeling bad¿ and was given unspecified medications.The patient declined to provide the blood glucose readings obtained in the hospital.The patient reported that he stayed in hospital for 2 days.At the time of troubleshooting, the cca walked through resolving the issue however the alleged issue could not be resolved.Replacement products were sent to the patient.This complaint is being reported because the patient reportedly required medical intervention and hospitalization after he was unable to test his blood glucose due to the error messages appearing and it is not known what medical treatment the patient received.

• Brand Name: ONETOUCH ULTRA2
• Common Device Name: GLUCOSE MONITORING SYS/KIT
• Manufacturer (Section D): LIFESCAN INC; 20 valley stream parkway; malvern PA 19355
• MDR Report Key: 21735497
• Report Number: 2939301-2025-00013
• Device Sequence Number: 12945392
• Product Code: NBW
• UDI-Device Identifier: 00353885011853
• UDI-Public: 00353885011853
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 03/31/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Lay User/Patient
• Device Model Number: 024-046
• Device Catalogue Number: 024-046
• Device Lot Number: Y2411030X
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 03/24/2025
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 03/31/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization
• Patient Sex: Unknown