MAUDE Adverse Event Report: ASPEN SURGICAL PRODUCTS, INC. CLASSIC PLUS® NEEDLE HOLDER, MICRO, W/CATCH, 8 3/4 IN, 222 MM

Model Number	36-1007
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device is in process of being returned for evaluation, and the investigation is ongoing.Once we have additional relevant information we will submit it in a supplemental report.
Event or Problem Description
Complainant alleges "purchased in (b)(6) 2023 one of the jaws has snapped off - sent to their own instrument repairer for assessment and cant be repaired".

• Brand Name: CLASSIC PLUS® NEEDLE HOLDER, MICRO, W/CATCH, 8 3/4 IN, 222 MM
• Common Device Name: NEEDLE HOLDER
• Manufacturer (Section D): ASPEN SURGICAL PRODUCTS, INC.; 6945 southbelt dr se; caledonia MI 49316
• Manufacturer Contact: terry hall ; 6945 southbelt dr se; caledonia, MI 49316 ; 6166987100
• MDR Report Key: 25363876
• Report Number: 3002750084-2026-00057
• Device Sequence Number: 18638252
• Product Code: GEN
• UDI-Device Identifier: 00887482009574
• UDI-Public: 00887482009574
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 06/24/2026

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
• Operator of Device: Health Professional
• Device Model Number: 36-1007
• Device Lot Number: 2180022856
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/04/2026
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 06/02/2026
• Supplement Report FDA Received Date: 06/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown