Centurion CR3145KRecalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

5 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.

Recalls naming this device

1. Sep 3, 2024Open, Classified

   Product has been identified as having holes in the packaging.

   Z-0133-2025 · Root cause: Device Design · FDA record ↗

2. May 23, 2023Open, Classified

   The kits incorrectly contain CirClamp subassembly 345CRSAK which results in the kits containing an incorrect bell and base size.

   Z-2649-2023 · Root cause: Process control · FDA record ↗

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-1407-2023 · Mar 2, 2023 · Open, Classified
  Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
• Z-0120-2020 · Aug 28, 2019 · Terminated
  Centurion 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 · Terminated
  Centurion 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-0836-05 · Apr 12, 2005 · Terminated
  Centurion brand CirClamp with 1.3 cm bell, sterile, single use; product 330.
• Z-0837-05 · Apr 12, 2005 · Terminated
  Centurion brand CirClamp with 1.1 cm bell, sterile, single use; product 310.