BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKN PICO 7

    MDR report key: 22055705 · Received May 20, 2025

    Report

    Report Number
    8043484-2025-00046
    Event Type
    Injury
    Date Received
    May 20, 2025
    Date of Event
    February 25, 2024
    Report Date
    May 20, 2025
    Manufacturer
    SMITH & NEPHEW MEDICAL LTD.
    Product Code
    OMP
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FI
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    INTERNAL REFERENCE NUMBER: (B)(4). LINDHOLM VM, SALMINEN AW, KOSKENMIES SJ, SALMIVUORI MK, HANNULA-JOUPPI KSE, ISOHERRANEN KM. AN EXPLORATORY RANDOMIZED CLINICAL TRIAL ON NEGATIVE PRESSURE WOUND THERAPY FOR LOWER LIMB FULL-THICKNESS SKIN GRAFTS OF DERMATOSURGICAL PATIENTS. INT WOUND J. 2024 JUN;21(6):E14911. DOI: 10.1111/IWJ.14911. PMID: 38831721; PMCID: PMC11148393. THIS COMPLAINT WAS OPENED BY SMITH+NEPHEW TO DOCUMENT A PATIENT COMPLICATION IDENTIFIED THROUGH A REVIEW OF CLINICAL EVIDENCE FROM LITERATURE SOURCES THAT INCLUDES REFERENCE TO THE USE OF A SMITH+NEPHEW PRODUCT. THE REPORTED ISSUE(S) RELATE TO KNOWN INHERENT PROCEDURAL RISKS THAT ARE APPROPRIATELY DOCUMENTED IN OUR RISK FILES. SMITH+NEPHEW WILL CONTINUE TO MONITOR TRENDS IN ACCORDANCE WITH OUR POST-MARKET SURVEILLANCE PROCESS AND TAKE NECESSARY ACTION AS REQUIRED IF ANTICIPATED SEVERITY AND/OR OCCURRENCE RATES ARE EXCEEDED. SMITH+NEPHEW HAS NO REASON TO SUSPECT THAT THE PRODUCT FAILED TO MEET ANY SPECIFICATIONS AT THE TIME OF MANUFACTURE. BASED ON OUR REVIEW OF ALL CURRENTLY AVAILABLE INFORMATION, WE ARE UNABLE TO CONFIRM A RELATIONSHIP BETWEEN THE REPORTED EVENT AND THE DEVICE OR IDENTIFY A DEFINITIVE ROOT CAUSE. HOWEVER, AS THE USE OF OUR PRODUCT CANNOT BE EXCLUDED AS A POTENTIAL CAUSE OR CONTRIBUTORY FACTOR TO THE REPORTED ISSUE, WE ARE CONSERVATIVELY SUBMITTING THIS REPORT IN ACCORDANCE WITH APPLICABLE REGULATIONS. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THAT ALTERS THE CONCLUSIONS OF THIS REPORT, A FOLLOW-UP REPORT WILL BE SUBMITTED AS REQUIRED.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT ON LITERATURE REVIEW "AN EXPLORATORY RANDOMIZED CLINICAL TRIAL ON NEGATIVE PRESSURE WOUND THERAPY FOR LOWER LIMB FULL-THICKNESS SKIN GRAFTS OF DERMATOSURGICAL PATIENTS", ONE (1) PATIENT SUSTAINED AN UNSPECIFIED INFECTION WITH NECROSIS WITHIN 3 MONTHS OF POST-OPERATIVE WOUND TREATMENT OF PATIENTS WHO UNDERGO FULL-THICKNESS SKIN GRAFT (FTSG) RECONSTRUCTIONS DUE TO LOWER LIMB SKIN CANCER, WHILE USING NEGATIVE PRESSURE WOUND THERAPY (NPWT) WITH PICO 7 DEVICE AND CUTICERIN DRESSING. IT IS UNKNOWN HOW PATIENT WAS TREATED. NO FURTHER INFORMATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26304 UNKN PICO 7 NEGATIVE PRESSURE WOUND THERAPY POWERED SUCTION PUMP OMP SMITH & NEPHEW MEDICAL LTD. UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other UNKN CUTICERIN