MEDLINE 67335Recalls & reported problems
Medline Industries, Inc. · DISP.UMBILICAL CORD CLAMP CUTTER(CTR300) · Class 1
- 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 10193489112696), received between Sep 9, 2026 and Sep 9, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Align” (1 report).
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
- Failure to Align1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2026Failure to Align
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50693360 ↗
Other INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC devices
- Colpassist M0068318210Boston Scientific Corporation · INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC1 recall2 reports
- Centurion 67335Centurion Medical Products Corporation · INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.