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    OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Black; Part Number: 72201996 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Blue; Part Number: 72201994 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    OSTEORAPTOR CURVED 2.3 mm Suture Anchor ULTRABRAID COBRAID Suture, Black; Part Number: 72203291 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.

    FDA Recall
    Terminated ·Crossroads Extremity Systems Llc·Product code JDR·February 16, 2017

    BIOMET TRAUMA Drill Bit, Tap, Guide Pin: [DVR Drill Bit, Item # 212000022, DVR 2.2MM DRILL BIT], [ALPS Drill Bit, Item # 214227160, 2.7X160MM CALIBRATED DRILL], [ALPS Drill Bit, Item # 824273100, 4.5X150MM DRILL], [ALPS Drill Bit, Item # 829029170, 2.5X140MM DRILL], [ALPS Drill Bit, Item # 829032170, 3.5X140MM DRILL], [ALPS Tap, Item # 824150170, 3.5X140MM CORTICAL TAP], [ALPS Guide Pin, Item # 829516150, 1.6X150MM BAYONET TIP GUIDE PIN], [ALPS Guide Pin, Item # 829516151, 1.6X150MM THREADED TIP GUIDE PIN]. Instruments are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDR·February 14, 2022

    Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code JDR·August 30, 2022

    OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture, White / Blue ; Part Number: 72201995 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    Nitinol Staple, Elastic Staple Large-Symmetrical, Sterile R, Model #: a) ES-18x14; b) ES-20x20; c) ES-25x22

    FDA Recall
    Terminated ·TriMed Inc.·Product code JDR·April 13, 2018

    Lupine BR Anchor w/Orthocord TCP/PLGA Absorbable Anchor, size 2 (5 metric) Braided Composite Suture, violet 36" (91cm) Size 2 (5metric) eyelet loop. Made in Switzerland; Sterile. The Lupine BR Anchor System is indicated for use in soft tissue bone fixation.

    FDA Recall
    Terminated ·DePuy Mitek, Inc., a Johnson & Johnson Co.·Product code JDR·April 29, 2008

    OSTEORAPTOR 2.3 mm Suture Anchor with ULTRABRAID COBRAID Suture, Blue; Part Number: 72201993 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    NeoSpan SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x10x10 UDI-DI Code: 00817906020083 T50 SN012 NeoSpan SuperElastic Compression Staple w/Instruments, Size 12x12x12 UDI-DI Code: 00817906020090 T50 SN020 NeoSpan SuperElastic Compression Staple w/Instruments, Size 20x20x20 UDI-DI Code: 00817906020151 T50 SN110 NeoSpan SuperElastic Compression Staple w/Instruments, Size 10x15x13 UDI-DI Code: 00817906020113 T50 SN115 NeoSpan SuperElastic Compression Staple w/Instruments, Size 15Wx15x15 UDI-DI Code: 00817906020137 T50 SN118 NeoSpan SuperElastic Compression Staple w/Instruments, Size 18x14x14 UDI-DI Code: 00810021861364 Single/multiple component metallic bone fixation appliances and accessories The In2Bones USA NeoSpan" Compression Staple Implant w/instruments is indicated for hand and foot bone fragments, osteotomy fixation and joint arthrodesis.

    FDA Recall
    Open, Classified ·In2bones USA, LLC·Product code JDR·May 11, 2026

    SPEED 15X12X12mm Continuous Compression Implant, Product No. SE-1512

    FDA Recall
    Open, Classified ·Synthes (USA) Products LLC·Product code JDR·September 27, 2022

    Nitinol Staple, Elastic Staple Small-Asymmetrical, Sterile R, Model #: a) ES-10x13x15; b) ES-10x16x19; c) ES-10x17x19; d) ES-12x13x15; e) ES-12x15x17; f) ES-12x16x19; g) ES-15x13x16

    FDA Recall
    Terminated ·TriMed Inc.·Product code JDR·April 13, 2018

    P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.

    FDA Recall
    Terminated ·Paragon 28, Inc.·Product code JDR·December 19, 2017

    BIOMET TRAUMA A.L.P.S. FIBULA COMPOSITE LOCKING PLATE 8 HOLE, Item # 856204008. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDR·February 14, 2022

    OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture, Black; Part Number: 72201992 Biodegradable suture anchor

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code JDR·August 6, 2013

    BIOMET Trauma, [Item # 13182-22-26, DVR CROSSLOCK EXTRA LONG PLATE LEFT], [Item # 1318-12-126, DVR CROSSLOCK EXTRA LONG PLATE RIGHT], [Item # 1318-12-176, DVR CROSSLOCK EXTRA EXTRA LONG PLATE RIGHT]. Devices are packaged in a vacuum sealed nylon pouch, which is placed in a carton with the appropriate IFU and patient record labels. Identifying labels on the pouch and the carton.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JDR·February 14, 2022

    Boston Scientific Vesica Sling Kits with Drill-In Anchor System sterile, for single use only; Ref/Catalog No. 820-100, UPN Product No. (M0068201000).

    FDA Recall
    Terminated ·Boston Scientific Corp·Product code JDR·June 2, 2006

    Stryker Vitallium Wire (6 Pack) Non Sterile. For use in bone procedures.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics Corp.·Product code JDR·December 23, 2015

    EasyFuse Dynamic Compression System Instrument Pack

    FDA Recall
    Terminated ·Wright Medical Technology, Inc.·Product code JDR·March 10, 2022