Unistik Touch AT 1424Recalls & reported problems
Owen Mumford Limited · Unistik Touch - Contact Activated Safety Lancet - 30G x 1.5mm - 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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00384701424014), received between Apr 26, 2019 and Apr 26, 2019 — classified as 2 injuries.
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
- Fail-Safe Problem2
- Protective Measures Problem2
Patient problems
- Anxiety2
- Needle Stick/Puncture2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 26, 2019Fail-Safe Problem; Protective Measures Problem; Fail-Safe Did Not Operate; Fail-Safe Problem; Protective Measures Problem; Fail-Safe Did Not Operate
TECHNICIAN TESTED A PATIENT AND DUE TO NON-RETRACTION, WAS ACCIDENTALLY PRICKED.
Patient problems: Anxiety; Needle Stick/Puncture
MAUDE report 8557824 ↗InjuryApr 26, 2019Fail-Safe Problem; Protective Measures Problem; Fail-Safe Did Not Operate; Fail-Safe Problem; Protective Measures Problem; Fail-Safe Did Not Operate
TECHNICIAN WAS PUTTING USED LANCET INTO SHARPS BIN AFTER TESTING PATIENT WHEN ACCIDENTAL PRICK OCCURRED.
Patient problems: Anxiety; Needle Stick/Puncture
MAUDE report 8557813 ↗
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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