MAUDE Adverse Event Report: Intrinsic Therapeutics, Inc Barricaid ACD

Model Number	BAR-A8-8mm
Medical Device Problem Code	Failure to Seal (4070)
Health Effect - Clinical Code	Hernia (2240)
Type of Reportable Event	Serious Injury
Event or Problem Description
Surgeon scheduled a re-operation for this patient due to a suspected re-herniation.Removal case was on (b)(6)2026 the device was removed prior to further surgical techniques and device was reported to be in good position.
Additional Manufacturer Narrative
The description of the events detailed in this mdr represent intrinsic therapeutic's understanding at the time of submission.If any further information is found which would change or alter any conclusions or new information submitted, another follow-up will be completed.Intrinsic therapeutics will continue to monitor for updates/trends.

• Brand Name: Barricaid ACD
• Common Device Name: Barricaid
• Manufacturer (Section D): Intrinsic Therapeutics, Inc; 30 commerce way; woburn MA 01801
• Manufacturer (Section G): Intrinsic Therapeutics, Inc; 30 commerce way; woburn MA 01801
• Manufacturer Contact: nicholas grow ; 30 commerce way; woburn, MA 01801 ; +1(781)932-0222
• MDR Report Key: 50165114
• Report Number: 3006232063-2026-00022
• Device Sequence Number: 15960659
• Product Code: QES
• UDI-Device Identifier: M906BARA88MM0
• UDI-Public: +M906BARA88MM0/$01052603/14D20290123E
• Combination Product (Y/N): N
• Initial Reporter State: KY
• Initial Reporter Country: US
• PMA/510(K) Number: P160050
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2026
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 08/06/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Operator of Device: Health Professional
• Device Model Number: BAR-A8-8mm
• Device Catalogue Number: 2730815-A8
• Device Lot Number: 01052603
• 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: 07/20/2026
• Initial Report FDA Received Date: 08/06/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 01/12/2026
• 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: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other; Required Intervention
• Patient Sex: Unknown