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 08/03/2016

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

Limited information was reported that a (b)(6) female patient underwent hernia repair surgery on or about (b)(6) 2015.The patient was implanted with a mesh product as part of the surgery.The records indicate this is a lifecell mesh.After surgery, the patient returned to the hospital on or about (b)(6) 2016 for a second mesh implant surgery.The patient returned to the hospital again on or about (b)(6) 2016 for a mesh revision operation.This record is associated with the report of a second mesh implanted.

Manufacturer Narrative

Internal investigation into strattice lot sp100350 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.Of 09/22/2022, of the (b)(4) devices released to finished goods for lot sp100350, (b)(4) have been distributed with (b)(4) 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 "sp100155-216 ((b)(6) 2015 implant) and sp100350-141 ((b)(6) 2016 implant)".No other information was reported.This record is associated with sp100350-141 ((b)(6) 2016 implant).As reported in the initial: limited information was reported that a 54 year old female patient underwent hernia repair surgery on or about (b)(6) 2015.The patient was implanted with a mesh product as part of the surgery.The records indicate this is a lifecell mesh.After surgery, the patient returned to the hospital on or about (b)(6) 2016 for a second mesh implant surgery.The patient returned to the hospital again on or about (b)(6) 2016 for a mesh revision operation.This record is associated with the report of a second mesh implanted.

• 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: 13580509
• MDR Text Key: 286646343
• Report Number: 1000306051-2022-00012
• 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: 10/04/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/22/2022
• 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: SP100350
• 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: 54 YR
• Patient Sex: Female