BD Microtainer® Quikheel™ Preemie Lancet 368100Recalls & reported problems
Becton, Dickinson And Company · LANCET QUIKHEEL PINK 0.85MMX1.75MM · 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 30382903681007), received between May 11, 2021 and Sep 27, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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 Contamination with Chemical or Other Material1
- Difficult or Delayed Activation1
- Illegible Information1
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.
MalfunctionSep 27, 2024Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT PRIOR TO USE OF THE BD MICROTAINER QUIKHEEL PREEMIE LANCET, THERE WAS FOREIGN MATTER OBSERVED ON ONE OF THE LANCET PACKAGES. THERE WERE NO HEALTH IMPACT OR CONSEQUENCES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20323562 ↗MalfunctionJul 11, 2023Illegible Information; Illegible Information
IT WAS REPORTED THAT WHILE USING BD MICROTAINER® QUIKHEEL¿ PREEMIE LANCET THERE WAS INCORRECT LABEL INFORMATION OF THREE LABELS. THREE LOT NUMBERS WERE AFFECTED. THERRE WAS NO REPORT OF PATIENT IMPACT. "WHEN THE BARCODES ON THE CASE BARCODE LABEL OF THE LOTS (CAT#368100/LOT#2259018, 2259021, 2291751) WERE READ BY KEYENCE SCANNERS, IT WAS POSSIBLE TO READ THEM, BUT THE LOT NUMBER AND THE EXPIRATION DATE WERE DETERMINED INCORRECTLY. AFTER CHECKING THE READ BARCODE INFORMATION, 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 17299205 ↗MalfunctionMay 11, 2021Difficult or Delayed Activation; Difficult or Delayed Activation
IT WAS REPORTED THAT BD MICROTAINER® QUIKHEEL¿ LANCET HAD A RETRACTION ISSUE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "THE NURSE FOUND THAT THE NEEDLE WASN'T COVERED BY SHIELD COMPLETELY PRIOR TO USE".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11809544 ↗
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- CARDINAL HEALTH SLMF200Cardinal Health 200, LLC · Lancet, blood16 reports
- BD Microtainer® Contact-Activated Lancet 366592Becton, Dickinson And Company · Single use only blood lancet with an integral sharps injury prevention feature14 reports
- Medline MPHSFTY28Medline Industries, Inc. · Single use only blood lancet with an integral sharps injury prevention feature6 reports
- Unistik Touch AT 1444Owen Mumford Limited · Lancet, Blood4 reports
- Unistik 3 AT 1012Owen Mumford Limited · Lancet, Blood3 reports
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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