BD Microtainer® QuikHeel™ Lancet 368101Recalls & reported problems
Becton, Dickinson And Company · LANCET QUIKHEEL TEAL 1.0MMX2.5MM · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 30382903681014), received between Sep 2, 2022 and May 9, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (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.
Reports received per month
Most reported problems
Device problems
- Device Markings/Labelling Problem1
- Missing Information1
- Product Quality Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 9, 2024Product Quality Problem; Product Quality Problem
IT WAS REPORTED THAT WHILE USING THE BD MICROTAINER® QUIKHEEL¿ LANCET THAT THE LANCET IS DEFECTIVE. PATIENT HAD TO BE RE-STUCK MULTIPLE TIMES. NO IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19277507 ↗MalfunctionJul 13, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT WHILE USING BD MICROTAINER® QUIKHEEL¿ LANCET, THE BARCODE WAS UNABLE TO BE READ CORRECTLY. THIS OCCURRED ON ONE LANCET. THERE WAS NO PATIENT IMPACT REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "ITT WAS POSSIBLE TO READ THE BARCODE, BUT THE LOT NUMBER AND THE EXPIRATION DATE WERE DETERMINED INCORRECTLY. IT WAS CONSIDERED THAT THE BARCODE COULD NOT BE IDENTIFIED CORRECTLY BECAUSE AN ILLEGAL CHARACTER "!" OR "T"WAS ENTERED AT THE END OF THE BARCODE NUMBER."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17317217 ↗MalfunctionSep 2, 2022Missing Information; Missing Information
IT WAS REPORTED WHEN USING THE BD MICROTAINER® QUIKHEEL¿ LANCET THERE WAS MISSING LABEL INFORMATION. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. THE CUSTOMER STATED: "THE SEARCHED SAMPLE OF LOT 1222506 DOES NOT PRESENT INSTRUCTIONS FOR USE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15352078 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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