MAUDE Adverse Event Report: KARL STORZ SE & CO. KG INNER SHEATH FOR 27050 SC

Model Number	27050CA
Medical Device Problem Codes	Break (1069); Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/23/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The affected device has been requested for investigation by the manufacturer.Device was not returned at the time of mdr submission.The event is filed under internal karl storz complaint id: (b)(4).
Event or Problem Description
It was reported that incident of fractures at the front-end ceramic head have occurred during hospital use.A ceramic head from a 27050ca detached and fell into a patient's bladder, leading to prolonged procedure time and increased patient risk.No negative impact in state of health reported.
Additional Manufacturer Narrative
New information received on october 14, 2025: initially anticipated surgery time (min): 40min prolongation (min): 60min due to this prolongation the case will be reported as adverse event.The event is filed under internal karl storz complaint id: (b)(4).
Additional Manufacturer Narrative
Device was returned to the manufacturing site as documented in section d9.This event is filed under internal complaint id (b)(4).
Additional Manufacturer Narrative
Result of investigation: after careful analysis of the available information and considering the instructions for use, it can be assumed that the breakage of the ceramic tip during the surgical procedure is due to a multifactorial process.The most likely cause is an application error in which the tip was mechanically overloaded.In addition, thermal influences such as insufficient distance between the electrode and the ceramic insert may have weakened the material.The instructions for use expressly point out that ceramic is a brittle material that is sensitive to mechanical and thermal stress.Even the smallest, initially invisible microcracks can grow through repeated stress (e.G., cleaning, sterilization) and eventually lead to breakage.An insufficient visual inspection before use and possible pre-existing damage from previous cycles may have contributed to the damage.Overall, everything indicates that mechanical stress and insufficient inspection prior to the procedure led to the failure of the ceramic tip.The event is filed under internal karl storz complaint id: (b)(4).

• Brand Name: INNER SHEATH FOR 27050 SC
• Common Device Name: INNER SHEATH FOR 27050 SC
• 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: 23301215
• Report Number: 9610617-2025-01812
• Device Sequence Number: 18648992
• Product Code: FJL
• UDI-Device Identifier: 04048551077412
• UDI-Public: 04048551077412
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K221893
• 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,User Facility,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 01/30/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 27050CA
• Device Catalogue Number: 27050CA
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/25/2025
• Supplement Date Received by Manufacturer: 10/14/2025; 12/10/2025; 01/28/2026
• Initial Report FDA Received Date: 10/15/2025
• Supplement Report FDA Received Date: 10/16/2025; 12/19/2025; 01/30/2026
• 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: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown