Centurion CIT5285Recalls & reported problems
Centurion Medical Products Corporation · Class 2
- 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 10653160246824), received between Jul 8, 2026 and Jul 8, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Dull, Blunt” (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
- Dull, Blunt1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 8, 2026Dull, Blunt
Patient problems: Pain
MAUDE report 25756630 ↗
Other Circumcision tray devices
- Medline Industries, Inc. DYNJ16826OMedline Industries, Inc. · Circumcision tray3 recalls0 reports
- Medline Industries, Inc. DYKMBNDL106Medline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL188Medline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. CIT5860Medline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL189AMedline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL106AMedline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. CIT5580Medline Industries, Inc. · Circumcision tray2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL189Medline Industries, Inc. · Circumcision tray2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.