Centurion CIT2590Recalls & reported problems
Centurion Medical Products Corporation · Class 2
Data updated Oct 13, 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 00653160020656), received between Sep 24, 2026 and Sep 24, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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 24, 2026Break
It was reported that "The scissors were broken during use. They separated."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884359 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page