MAUDE Adverse Event Report: INTEGRA - PRINCETON MICROMYST APPLICATOR BOX OF 5; SEALANT APPLICATORS

Catalog Number	205000DS
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
An investigation has been initiated based on the reported information.Upon completion of the investigation, a follow-up report will be submitted.
Event or Problem Description
This is 1 of 4 reports linked to mfg report numbers: 3003418325-2025-00025, 3003418325-2025-00027, 3003418325-2025-00028.A facility returned voluntary medical device recall letter and indicated that they are investigating four micromyst applicator box of 5 (205000ds) with known infections after use of the product.Additional information has been requested.
Additional Manufacturer Narrative
Additional information: 1.Please advise the type of infection/organism if known.¿ craniotomy deep surgical site infection, organism cutibacterium acnes ¿ craniotomy deep surgical site infection, organism cutibacterium acnes, staphylococcus coag negative, staphylococcus lugdunensis ¿ craniotomy deep surgical site infection, organism staphylococcus aureus ¿ craniotomy organ space surgical site infection, organism cutibacterium acnes.2.What tests were done to confirm the infection in the patient? ¿ organism identified from fluid or tissue in the deep and/or organ space by culture or non-cultured microbiologic testing ¿ physician assessment that may include gross anatomical exam, histopathologic exam and/or imaging test ¿ surgical site infection in-depth review by an infection preventionist.3.What treatment and or medication was given for the infection ¿ if medications were administered, please include medication names.¿ i do not have access to provider to patient treatment plans or outcomes.4.Please advise if any other medical/surgical intervention was administered.¿ i do not have access to provider to patient treatment plans or outcomes.5.What is the health history of the patient? ¿ 3 patients are clinically obese, and 1 had diabetes.6.Please advise of the patient¿s outcome and/or status regarding the infection.¿ i do not have access to provider to patient treatment plans or outcomes.A notable finding was that our microbiology department cultured several sterile unused/unopened product that had been pulled from service.One of the cultures resulted in: organism cutibacterium acnes.Investigation findings: the micromyst applicator box of 5 (205000d) was not returned for analysis as only a dhr review could be performed.At the time of manufacturing, records from each manufacturing lot are thoroughly reviewed to ensure that products are released meeting all quality release specifications.The dhr review confirmed the finished good for the work order was processed within qualified parameters and passed the required inspection checks.The root cause is undetermined and was unable to be confirmed in the complaint evaluation.Per the fmea, potential causes of failure include: biocompatibility.The risk remains acceptable per the risk analysis.No enhancements or improvements were generated for the reported condition.Trends will be monitored for this and similar issues.At present, we consider this complaint to be closed.If additional information becomes available in the future, this complaint will be reopened, and the respective evaluation performed.
Event or Problem Description
N/a.

• Brand Name: MICROMYST APPLICATOR BOX OF 5
• Common Device Name: SEALANT APPLICATORS
• Manufacturer (Section D): INTEGRA - PRINCETON; 1100 campus road; 1100 campus road; princeton NJ 08540
• Manufacturer (Section G): INTEGRA - PRINCETON; 1100 campus road; none; princeton NJ 08540
• Manufacturer Contact: vivian nelson ; 1100 campus drive; princeton, NJ 08540 ; 6099362319
• MDR Report Key: 22302435
• Report Number: 3003418325-2025-00026
• Device Sequence Number: 12909969
• Product Code: FMF
• UDI-Device Identifier: 10381780000112
• UDI-Public: 10381780000112
• Combination Product (Y/N): N
• PMA/510(K) Number: K082454
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Remedial Action: Recall
• Type of Report: Initial,Followup
• Report Date (Section B): 08/25/2025

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 Catalogue Number: 205000DS
• Device Lot Number: 2023120403
• 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: 06/03/2025
• Supplement Date Received by Manufacturer: 07/31/2025
• Initial Report FDA Received Date: 06/20/2025
• Supplement Report FDA Received Date: 08/25/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: 3003418325/05/23/2025/R/
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown