CARDINAL HEALTH SLULF200Recalls & reported problems
Cardinal Health 200, LLC · ULTRA LOW FLOW SAFETY LANCET, 30G, · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20885380065955), received between Jul 27, 2023 and Jul 27, 2023 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Retraction Problem” (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
- Retraction Problem2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 27, 2023Retraction Problem; Retraction Problem
OMI'S CUSTOMER CARDINAL HEALTH EMAILED THEIR EVENT FORM TO REPORT THEIR CUSTOMER, (B)(6)HOSPITAL HAD A LANCET NOT RETRACT AFTER USING ON A FINGERSITCK AND AS A RESULT THE RN PERFORMING THE PROCEDURE WAS STUCK WITH THE USED NEEDLE.
Patient problems: Insufficient Information
MAUDE report 17406381 ↗InjuryJul 27, 2023Retraction Problem; Retraction Problem
CUSTOMER EMAILED WITH EVENT FORM TO REPORT THAT THEIR CUSTOMER BARNES JEWISH HOSPITAL HAD A LANCET NOT RETRACT AFTER USING ON A FINGERSTICK AND AS A RESULT THE RN PERFORMING THE PROCEDURE WAS STUCK WITH THE USED NEEDLE.
Patient problems: Insufficient Information
MAUDE report 17406380 ↗
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- 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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