MAUDE Adverse Event Report: KARL STORZ SE & CO. KG ANATOMICAL BLADE, SHORT

Model Number	26159UHW
Medical Device Problem Codes	Break (1069); Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the open/close function of the grasping no longer works.The pin is missing.No negative impact in state of health reported.
Additional Manufacturer Narrative
The device in question was returned to the manufacturer.The evaluation is anticipated, but not yet begun.The investigation will be performed by a designated karl storz employee.The event is filed under internal karl storz complaint id: (b)(4).
Additional Manufacturer Narrative
Investigation: a connecting rivet has come loose in the joint on the distal side.This is due to a manufacturing defect (investigation carried out by the supplier).The weld seam on the back part was not deep enough.An employee did not drill the hole deep enough.The following information can be found in the manufacturer's 8d report (b)(4)."main cause / causes: rivet has come loose, weld on the jaw part not deep enough, countersink on the jaw part too small, employee did not countersink correctly".The corresponding operating instructions ri: 26159bhw_en_v48.2_03-2023_ri_ce refer to a visual and functional inspection of the device on pages 14 and 16.The operating instructions 97000045 v2.0 - 10/2017 state that overloading should be avoided, see page 2.The event is filed under internal karl storz complaint id: (b)(4).

• Brand Name: ANATOMICAL BLADE, SHORT
• Common Device Name: ANATOMICAL BLADE, SHORT
• Manufacturer (Section D): KARL STORZ SE & CO. KG; dr.-karl-storz-strasse 34; tuttlingen, 78532 ; GM 78532
• Manufacturer (Section G): KARL STORZ SE & CO. KG; dr.-karl-storz-strasse 34; tuttlingen, 78532 ; GM 78532
• Manufacturer Contact: anja fair ; 2151 e grand ave; el segundo, CA 90245
• MDR Report Key: 23066900
• Report Number: 9610617-2025-01598
• Device Sequence Number: 21284278
• Product Code: GCJ
• UDI-Device Identifier: 04048551094495
• UDI-Public: 04048551094495
• Combination Product (Y/N): N
• Initial Reporter Country: GM
• PMA/510(K) Number: K934937
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 03/12/2026

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: 26159UHW
• Device Catalogue Number: 26159UHW
• Device Lot Number: RL01
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/18/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/28/2028
• Supplement Date Received by Manufacturer: 02/19/2026
• Initial Report FDA Received Date: 09/16/2025
• Supplement Report FDA Received Date: 03/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown