MAUDE Adverse Event Report: Centurion Medical Products, LP CENTURION; CIRCLAMP W/1.1CM BELL (ST)

Catalog Number	310CR
Medical Device Problem Code	Damaged Thread (4075)
Health Effect - Clinical Code	Skin Tears (2516)
Date of Event	12/17/2024
Type of Reportable Event	Malfunction

• Brand Name: CENTURION
• Common Device Name: CIRCLAMP W/1.1CM BELL (ST)
• Manufacturer (Section D): Centurion Medical Products, LP; 301 catrell drive; howell MI 48843 -170
• Manufacturer Contact: shirisha mothe ; three lakes drive; northfield, IL 60093--275
• MDR Report Key: 50938589
• Report Number: 1824619-2026-00143
• Device Sequence Number: 10756164
• Product Code: HFX
• UDI-Device Identifier: 00653160197471
• UDI-Public: 00653160197471
• Combination Product (Y/N): N
• Initial Reporter State: OK
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/28/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: 310CR
• Device Lot Number: 2024090401
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 12/19/2024
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/17/2024
• Initial Report FDA Received Date: 09/29/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown