Medline MPHSFTY28Recalls & reported problems
Medline Industries, Inc. · LANCET,SAFETY,28G,1.6MM,PUSH BUTTON · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00193489006448), received between Sep 22, 2026 and Sep 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Dull, Blunt4
- Material Integrity Problem1
- Separation Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950183 ↗MalfunctionSep 24, 2026Material Integrity Problem
It was reported that "NEEDLE IS NOT COMING OUT OF DEVICE. PRODUCT IS DEFECTIVE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884519 ↗MalfunctionSep 23, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50873874 ↗MalfunctionSep 23, 2026Separation Failure
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872724 ↗MalfunctionSep 23, 2026Dull, Blunt
It was reported that "I tried 5 times (5 lancets) last week and pressed them against my finger and pressed down on the plunger on back. It produced a click but no puncture and no blood".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50868673 ↗MalfunctionSep 22, 2026Dull, Blunt
It was reported that "I tried 5 times (5 lancets) last week and pressed them against my finger and pressed down on the plunger on back. It produced a click but no puncture and no blood".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854086 ↗
Other Single use only blood lancet with an integral sharps injury prevention feature devices
- BD Microtainer® Contact-Activated Lancet 366593Becton, Dickinson And Company · Lancet, blood89 reports
- BD Microtainer® Contact-Activated Lancet 366594Becton, Dickinson And Company · Lancet, blood64 reports
- OneTouch Ultrasoft 020-393LifeScan Europe GmbH · Lancet, Blood1 recall0 reports
- 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
- Unistik Touch AT 1444Owen Mumford Limited · Lancet, Blood4 reports
- BD Microtainer® QuikHeel™ Lancet 368101Becton, Dickinson And Company · Single use only blood lancet with an integral sharps injury prevention feature3 reports
- LEADER 4817904Cardinal Health 110, Inc. · 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page