OneTouch Verio 024-269Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00353885012614), received between Oct 28, 2025 and Oct 28, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Use of Device Problem” (2 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryOct 28, 2025Use of Device Problem; Use of Device Problem

  ON (B)(6) 2025, THE LAY USER/PATIENT CONTACTED LIFESCAN (LFS) USA, ALLEGING A PRODUCT USABILITY ISSUE WITH THEIR ONE TOUCH VERIO TEST STRIPS. THIS COMPLAINT WAS CLASSIFIED BASED ON INFORMATION OBTAINED BY THE CUSTOMER CARE AGENT (CCA) DURING THE INITIAL CALL. THE PATIENT REPORTED THAT THE ALLEGED ISSUE OCCURRED AT AROUND 7:30 A.M., ON (B)(6) 2025. THE PATIENT MANAGES THEIR DIABETES WITH ORAL MEDICATION (METFORMIN, 500 MG IN THE EVENING; FARXIGA, 5 MG DAILY AND, GLYBURIDE, 5 MG TWICE DAILY). THE PATIENT ADVISED THAT THEY WOKE UP AND ¿ACCIDENTALLY INGESTED SOME STRIPS¿, APPROXIMATELY ¿7 TO 10¿ TEST STRIPS AS THEY HAD CONFUSED THE TEST STRIP VIAL WITH A MEDICINE BOTTLE. THE PATIENT ADVISED THAT IN RESPONSE TO INGESTING THE TEST STRIPS, THEY ATTEMPTED TO VOMIT AND ATE A SMALL PIECE OF BREAD. THE PATIENT REPORTED THAT THEY NOTICED THAT THEIR ¿PHLEGM FELT DIFFERENT ¿ NOT NORMAL¿ AND DESCRIBED HAVING A ¿METALLIC AND CHEMICAL¿ TASTE. THE PATIENT WENT TO THE EMERGENCY ROOM AT AROUND 9 A.M., ON (B)(6) 2025, WHERE THEY RECEIVED IV FLUIDS, WERE PLACED ON CARDIAC MONITORING, HAD SOME LAB SAMPLES TAKEN AND HAD A CHEST X-RAY. THE PATIENT REQUESTED TEST STRIP INFORMATION WHICH THE CCA PROVIDED. TH

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23402955 ↗
• InjuryOct 28, 2025Use of Device Problem; Use of Device Problem

  ON (B)(6) 2025, THE LAY USER/PATIENT CONTACTED LIFESCAN (LFS) USA, ALLEGING A PRODUCT USABILITY ISSUE WITH THEIR ONE TOUCH VERIO TEST STRIPS. THIS COMPLAINT WAS CLASSIFIED BASED ON INFORMATION OBTAINED BY THE CUSTOMER CARE AGENT (CCA) DURING THE INITIAL CALL. THE PATIENT REPORTED THAT THE ALLEGED ISSUE OCCURRED AT AROUND 7:30 A.M., ON (B)(6) 2025. THE PATIENT MANAGES THEIR DIABETES WITH ORAL MEDICATION (METFORMIN, 500 MG IN THE EVENING; FARXIGA, 5 MG DAILY AND, GLYBURIDE, 5 MG TWICE DAILY). THE PATIENT ADVISED THAT THEY WOKE UP AND ¿ACCIDENTALLY INGESTED SOME STRIPS¿, APPROXIMATELY ¿7 TO 10¿ TEST STRIPS AS THEY HAD CONFUSED THE TEST STRIP VIAL WITH A MEDICINE BOTTLE. THE PATIENT ADVISED THAT IN RESPONSE TO INGESTING THE TEST STRIPS, THEY ATTEMPTED TO VOMIT AND ATE A SMALL PIECE OF BREAD. THE PATIENT REPORTED THAT THEY NOTICED THAT THEIR ¿PHLEGM FELT DIFFERENT ¿ NOT NORMAL¿ AND DESCRIBED HAVING A ¿METALLIC AND CHEMICAL¿ TASTE. THE PATIENT WENT TO THE EMERGENCY ROOM AT AROUND 9 A.M., ON (B)(6) 2025, WHERE THEY RECEIVED IV FLUIDS, WERE PLACED ON CARDIAC MONITORING, HAD SOME LAB SAMPLES TAKEN AND HAD A CHEST X-RAY. THE PATIENT REQUESTED TEST STRIP INFORMATION WHICH THE CCA PROVIDED. TH

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23402907 ↗