BEUDAMED
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    SYNOVIS SURGICAL INNOVATION

    FDA Adverse Event
    Malfunction ·SYNOVIS LIFE TECHNOLOGIES·Product code FTL·February 25, 2004

    VASCULAR PROBE

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code FKA·July 25, 2006

    DURASEAL DURAL SEALANT SYSTEM

    FDA Adverse Event
    Injury ·CONFLUENT SURGICAL·Product code NQR·July 27, 2007

    NEUROTUBE

    FDA Adverse Event
    Injury ·NEUROREGEN L.L.C.·Product code JXI·May 16, 2008

    NEUROTUBE

    FDA Adverse Event
    Injury ·NEUROREGEN L.L.C.·Product code JXI·May 16, 2008

    DURASEAL DURAL SEALANT SYSTEM

    FDA Adverse Event
    Injury ·CONFLUENT SURGICAL·Product code NQR·July 27, 2007

    COUPLER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code MVR·February 11, 2019

    Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSDV), sterile EO, Rx Only, Synovis Surgical Innovations, A Division of Synovis Life Technologies, Inc, 2575 University Ave W., St Paul, MN 55114-1024. The device is intended to be used as a staple line buttress

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code FTM·October 26, 2011

    PSD Gel that's provided with Peri-Strips Dry Staple Line Reinforcement with Apex Processing (PSD) and Peri-Strips Dry with Veritas Collagen Matrix Staple Line Reinforcement (PSD-V) products. Sterile, Rx only, Synovis Surgical Innovations. Intended to be used as a staple line buttress.

    FDA Recall
    Terminated ·Synovis Surgical Inovation Div. of·Product code DXZ·June 30, 2010

    GEM NEUROTUBE

    FDA Adverse Event
    Other ·SYNOVIS SURGICAL INNOVATIONS·Product code JXI·July 12, 2013

    VERITAS COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·April 12, 2014

    VERITAS COLLAGEN MATRIX

    FDA Adverse Event
    Injury ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·June 18, 2014

    PERI-STRIP

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·October 20, 2016

    FLO-THRU

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DXC·December 22, 2016

    VASCULAR PROBE

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DWP·December 22, 2016

    GEM MICROVASCULAR ANASTOMOTIC COUPLER

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code MVR·October 11, 2016

    FLO-THRU

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DXC·December 22, 2016

    PERI-STRIP

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code FTM·October 20, 2016

    VASCULAR PROBES

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DWP·July 16, 2015

    FLO-THRU

    FDA Adverse Event
    Malfunction ·SYNOVIS SURGICAL INNOVATIONS·Product code DXC·August 12, 2015