Unistik Touch AT 1414Recalls & reported problems
Owen Mumford Limited · Unistik Touch - Contact Activated Safety Lancet - 21G x 2.0mm - 200 count - sterile, single use safety lancet. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00384701414015), received between Sep 12, 2022 and Sep 12, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (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 18, 2026.
Most reported problems
Device problems
- Fail-Safe Did Not Operate2
Patient problems
- Exposure to Body Fluids2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 12, 2022Fail-Safe Did Not Operate; Fail-Safe Did Not Operate
HOSPITAL REPORTED TO MEDSUM THAT WHEN TAKING THE PATIENT'S BLOOD SUGAR, LANCET USED DID NOT RETRACT. WHEN REMOVED AWAY FROM PATIENT, NEEDLE EXPOSED AND PENETRATED THROUGH GLOVE RESULTING IN NEEDLE STICK.
Patient problems: Exposure to Body Fluids
MAUDE report 15407205 ↗MalfunctionSep 12, 2022Fail-Safe Did Not Operate; Fail-Safe Did Not Operate
HOSPITAL REPORTED TO MEDSUM THAT WHEN TAKING THE PATIENT'S BLOOD SUGAR, LANCET USED DID NOT RETRACT. WHEN REMOVED AWAY FROM PATIENT, NEEDLE EXPOSED AND PENETRATED THROUGH GLOVE RESULTING IN NEEDLE STICK.
Patient problems: Exposure to Body Fluids
MAUDE report 15407178 ↗
Other Lancet, Blood 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
- 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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