Centurion 330CRRecalls & reported problems
Centurion Medical Products Corporation · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00653160197495), received between Jun 12, 2026 and Jun 12, 2026 — classified as 1 malfunction.
1 FDA recall record name this device's identifier, 1 still open.
6 other recalls cover devices cleared under the same FDA submission (K890897); they may or may not involve this specific model.
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
Recalls naming this device
- Sep 3, 2024Open, Classified
Product has been identified as having holes in the packaging.
Z-0133-2025 · Root cause: Device Design · FDA record ↗
Most reported problems
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.
MalfunctionJun 12, 2026
A DISPOSABLE CENTURION 1.3 CLAMP WAS USED FOR A CIRCUMCISION. WHEN THE BELL WAS BEING REMOVED FROM THE HEAD OF THE PENIS, A METAL SHARD ADHERED TO THE GLANS. THE OB NOTED THIS SHARD AND PREVENTED INJURY FROM INFANT'S CIRCUMCISION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25485429 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K890897. One submission often covers many models, so check the product and lot details in each record.
- Z-2649-2023 · May 23, 2023 · Open, ClassifiedCenturion Sterile CirClamp with 1.45cm Bell Reprocessed, Reorder CR3145K, 1 per package, 12 per case.
- Z-1407-2023 · Mar 2, 2023 · Open, ClassifiedCenturion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
- Z-0120-2020 · Aug 28, 2019 · TerminatedCenturion CIRCLAMP W/1.1CM BELL - single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. ReOrder: 310CR
- Z-0121-2020 · Aug 28, 2019 · TerminatedCenturion CIRCLAMP W/1.3 CM BELL-single-use, disposable instrument used to compress the foreskin of the penis during circumcision of a male infant. ReOrder: 330CR
- Z-0837-05 · Apr 12, 2005 · TerminatedCenturion brand CirClamp with 1.1 cm bell, sterile, single use; product 310.
- Z-0836-05 · Apr 12, 2005 · TerminatedCenturion brand CirClamp with 1.3 cm bell, sterile, single use; product 330.
Other CLAMP, CIRCUMCISION devices
- Centurion CR3145KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION2 recalls0 reports
- Centurion CR230KCenturion Medical Products Corporation · CLAMP, CIRCUMCISION2 recalls0 reports
- Centurion 330CRKCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall8 reports
- Centurion 310CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall4 reports
- Centurion 230CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 210CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 200CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 reports
- Centurion 245CRCenturion Medical Products Corporation · CLAMP, CIRCUMCISION1 recall0 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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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