TRUEplus Good Neighbor Pharmacy TRUEplus Sterile Lancets (REF S1011MC33-100)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00087701426063), received between Feb 18, 2022 and Jan 13, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Dull, Blunt” (1 report).

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 18, 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.

• MalfunctionJan 13, 2026Dull, Blunt

  CONSUMER REPORTED COMPLAINT FOR THE TRUEPLUS LANCETS, STATING THAT SOME OF THE LANCETS FROM THE BOX HE IS CURRENTLY USING ARE DULL. PER THE CUSTOMER THE PACKAGE HAD NOT BEEN OPEN OR DAMAGED WHEN RECEIVED. THE CUSTOMER FIRST USED THE PRODUCT OUT OF THIS PACKAGE ABOUT 2 MONTHS AGO. AT THE TIME OF THE CALL THE CUSTOMER FELT WELL AND DID NOT REPORT ANY SYMPTOMS. THE CUSTOMER IS NOT CLAIMING THEY WERE INJURED USING THE LANCETS AND NO MEDICAL INTERVENTION RELATED TO THE USE OF THE PRODUCT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24058992 ↗
• MalfunctionFeb 18, 2022Material Twisted/Bent; Material Twisted/Bent

  CONSUMER REPORTED COMPLAINT FOR THE TRUEPLUS 33G LANCETS. CUSTOMER STATED THAT BOTH THE LANCETS AND THE LANCET NEEDLES WERE BENT. THE PACKAGE HAD NOT BEEN OPEN OR DAMAGED WHEN RECEIVED BY THE CUSTOMER. THE CUSTOMER HAS BEEN USING THE LANCETS OUT OF THIS PACKAGE FOR ONE MONTH. THE CUSTOMER FEELS WELL AND DID NOT REPORT ANY SYMPTOMS. NO MEDICAL ATTENTION ASSOCIATED WITH THE USE OF THE PRODUCT WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13558530 ↗