Medline MPHPRESS30Recalls & reported problems
Medline Industries, Inc. · LANCET,SAFETY,30G,1.5MM, PRESSURE · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30884389103023), received between Sep 17, 2024 and Sep 17, 2024 — classified as 1 malfunction.
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 16, 2026.
Reports received per month
Most reported problems
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2024
PATIENT WITH TYPE 1 DIABETES MELLITUS; LANCET USED TO DRAW FOR BLOOD SUGARS SLICED PATIENT'S FINGER (NO OTHER DESCRIPTIONS AVAILABLE) AND STAFF SAID SIMILAR OCCURRENCES LATELY - THIS SPECIFIC DEVICE NOT SAVED BUT TEAM PRESENTED SAFETY REPORT TO TRACK & TREND AND THEY SAVED THE BALANCE OF THE LANCETS IN THE BOX FROM WHICH THEY PROCURED SUBJECT LANCET. NO RESIDUAL ISSUE NOR INJURY TO PATIENT AND NO TREATMENT NOTED.
Patient problems: Laceration(s)
MAUDE report 20236273 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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