MAUDE Adverse Event Report: Medtronic Dominicana BioGlide®; SHUNT, CENTRAL NERVOUS SYSTEM AND COMPONENTS

Model Number	93522
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Hypersensitivity/Allergic reaction (1907); Inflammation (1932)
Date of Event	08/12/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
Medtronic received information regarding a catheter.It was reported that the ventriculoperitoneal shunt was intended to drain cerebrospinal fluid in a patient with hydrocephalus, relieve the symptoms of hydrocephalus, and reduce intracranial pressure.Its clinical indications included obstructive hydrocephalus, communicating hydrocephalus, and other conditions requiring cerebrospinal fluid diversion.The patient had a clinical indication for ventriculoperitoneal shunt surgery because of hydrocephalus.On (b)(6) 2026, cranioplasty and ventriculoperitoneal shunt surgery were performed under general anesthesia, and the shunt was implanted.A rejection reaction/inflammation could have occurred after implantation.The patient's intracranial inflammatory response was controlled, cerebrospinal fluid inflammatory indicators were monitored dynamically, and the medical device adverse event was reported.Date of improvement was (b)(6) 2026.
Additional Manufacturer Narrative
Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: BioGlide®
• Common Device Name: SHUNT, CENTRAL NERVOUS SYSTEM AND COMPONENTS
• Manufacturer (Section D): Medtronic Dominicana; zona franca de san isidro; carretera san isidro, km 17; santo domingo 11500 ; DR 11500
• Manufacturer (Section G): Medtronic Dominicana; zona franca de san isidro; carretera san isidro, km 17; santo domingo 11500 ; DR 11500
• Manufacturer Contact: justin ellis ; 4620 n. beach st.; fort worth, TX 76137 ; +1(763)526-5677
• MDR Report Key: 50754140
• Report Number: 9612501-2026-02511
• Device Sequence Number: 9668042
• Product Code: JXG
• UDI-Device Identifier: 00763000027605
• UDI-Public: (01)00763000027605(17)300222(10)0231393380
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K792005
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 09/14/2026

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: 93522
• Device Catalogue Number: 93522
• Device Lot Number: 0231393380
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/02/2026
• Initial Report FDA Received Date: 09/14/2026
• Date Device Manufactured: 05/19/2025
• 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
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 61 YR
• Patient Sex: Male