MAUDE Adverse Event Report: Dornier MedTech Systems GmbH Dornier Delta III; Lithotripter

Model Number	Dornier Delta III
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Rupture (2208)
Date of Event	04/23/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
Patient splenic rupture was reported to have occured following a procedure utilizing a dornier delta iii sn: (b)(6).

• Brand Name: Dornier Delta III
• Common Device Name: Lithotripter
• Manufacturer (Section D): Dornier MedTech Systems GmbH; argelsrieder feld 7; wessling, D-822 34; GM D-82234
• MDR Report Key: 50241365
• Report Number: 50241365
• Device Sequence Number: 10329402
• Product Code: LNS
• UDI-Device Identifier: 04049957005429
• UDI-Public: (01)04049957005429
• Combination Product (Y/N): N
• Initial Reporter State: MO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: User Facility
• Type of Report: Initial
• Report Date (Section B): 08/13/2026
• Report Date (Section F): 08/13/2026

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?: No
• Operator of Device: Health Professional
• Device Model Number: Dornier Delta III
• Device Catalogue Number: K1039062
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 07/24/2026
• Device Age: 6 YR
• Event Location: Hospital
• Date Report to Manufacturer: 08/13/2026
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/13/2026
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown
• Date Report Sent to FDA: 08/13/2026