MAUDE Adverse Event Report: STRATTICE RECONSTRUCTIVE TISSUE MATRIX, 10 X 16, FIRM; MESH, SURGICAL

Catalog Number 1016002

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Hernia (2240)

Event Date 09/21/2016

Event Type  Injury  

Manufacturer Narrative

This legal event is being reported as serious injury due to the reported recurrence with surgical intervention.The lot associated with this event was not reported and remains unknown; therefore a review of the device history records could not be performed.No strattice devices were returned for evaluation.Based on the limited information reported, a relationship between the event and strattice cannot be confirmed.Due to the legal process, if additional information is made available during legal proceedings, a supplemental report will be submitted.

Event Description

It was reported through a legal event that a (b)(6) year old female underwent hernia repair surgery on or about (b)(6) 2015.During the hernia repair surgery, the surgeon implanted a strattice firm mesh.After surgery, the patient returned to the hospital on or about (b)(6) 2016.And was diagnosed with ventral hernia recurrence.On or about (b)(6) 2016, the patient underwent a recurrent ventral hernia repair with bilateral rectus muscle flaps, adhesion removal from intestines, and excision of old mesh.

Manufacturer Narrative

Internal investigation into strattice lot sp100220 included a review of the reported information, review of the device history records, and a review of the complaint history records.The investigation resulted in no remarkable findings, including no other complaints reported against the lot and no deviations or related non-conformances revealed during processing.The lot was terminally sterilized within the process parameters and met all qc release criteria.As of 09/22/2022, of the (b)(4) devices released to finished goods for lot sp100220, 203 have been distributed with 122 reported as implanted.Based on our internal investigation with no remarkable findings, and without relevant patient factors, a relationship between the strattice and this event could not be determined.Due to the legal process, if additional information is made available during legal proceedings, a supplemental report will be submitted.As reported in the initial: this legal event is being reported as serious injury due to the reported recurrence with surgical intervention.The lot associated with this event was not reported and remains unknown; therefore a review of the device history records could not be performed.No strattice devices were returned for evaluation.Based on the limited information reported, a relationship between the event and strattice cannot be confirmed.Due to the legal process, if additional information is made available during legal proceedings, a supplemental report will be submitted.

Event Description

This is follow up #1 to report on september 14th, 2022, pmqa received notification from legal that the lot associated with this event was found through discovery and are sp100220-093.No other information was reported.As reported in the initial: it was reported through a legal event that a 58 year old female underwent hernia repair surgery on or about (b)(6) 2015.During the hernia repair surgery, the surgeon implanted a strattice firm mesh.After surgery, the patient returned to the hospital on or about (b)(6) 2016.And was diagnosed with ventral hernia recurrence.On or about (b)(6) 2016, the patient underwent a recurrent ventral hernia repair with bilateral rectus muscle flaps, adhesion removal from intestines, and excision of old mesh.

• Brand Name: STRATTICE RECONSTRUCTIVE TISSUE MATRIX, 10 X 16, FIRM
• Type of Device: MESH, SURGICAL
• Manufacturer Contact: christopher belle ; 1 millennium way; branchburg, NJ 08876 ; 9089471470
• MDR Report Key: 13685634
• MDR Text Key: 288672170
• Report Number: 1000306051-2022-00030
• Device Sequence Number: 1
• Product Code: FTM
• UDI-Device Identifier: 00818410010119
• UDI-Public: 00818410010119
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K070560
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Company Representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 10/03/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/07/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 1016002
• Device Lot Number: SP100220
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 09/14/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: NO INFORMATION REPORTED.
• Patient Outcome(s): Required Intervention
• Patient Age: 58 YR
• Patient Sex: Female