BEUDAMED
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    UroPass Ureteral Access Sheaths, 5 pieces/box

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code KNY·May 19, 2023

    Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014

    FDA Recall
    Open, Classified ·DeRoyal Industries Inc·Product code FNY·May 30, 2023

    Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access Sheaths Model/Catalog Number: 61024BX, 61038BX, 61046BX, 61054BX, 61124BX, 61138BX, 61146BX, 61154BX, 61224BX, 61238BX, 61246BX, 61254BX, 61324BX, 61338BX, 61346BX, 61354BX Software Version: N/A Product Description: The Olympus UroPass Ureteral Access Sheath Set consists of a hydrophilic coated outer sheath and an inner tapered dilator intended to establish a conduit for the passage of endoscopes and retrieval devices into the ureter. The hydrophilic coating on the UroPass Ureteral Access Sheath eases passage and placement. Both the outer sheath and inner dilator are radio-opaque for ease of viewing radiographically. Intended for single use only. Component: N/A

    FDA Recall
    Open, Classified ·Olympus Corporation of the Americas·Product code KNY·September 11, 2024

    Scooter

    FDA Recall
    Open, Classified ·Merits Holdings Co. dba Merits Health Products, Inc.·Product code INI·April 1, 2021

    Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) 00816125023653(10) EBL10B13C(17) 270630 Tribio" Implant is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure.

    FDA Recall
    Open, Classified ·Berkeley Advanced Biomaterials, LLC·Product code MQV·September 2, 2025

    Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614

    FDA Recall
    Open, Classified ·Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany·Product code GWO·March 29, 2024

    VACUETTE TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

    FDA Recall
    Open, Classified ·Greiner Bio-One North America, Inc.·Product code JKA·May 14, 2024

    Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product Description: Greiner VACUETTE Blood Collection Tube with Clot Activator and Gel Separator and Standard Stopper (16 x 100 mm, 8ml)

    FDA Recall
    Open, Classified ·Greiner Bio-One North America, Inc.·Product code JKA·August 19, 2025

    Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2%, REF: 454322

    FDA Recall
    Open, Classified ·Greiner Bio-One North America, Inc.·Product code GIM·August 8, 2025

    VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, non-ridged.

    FDA Recall
    Open, Classified ·Greiner Bio-One North America, Inc.·Product code JKA·December 12, 2023

    MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782120

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782110

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782103

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Ingenia Ambition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782109

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782105

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.

    FDA Recall
    Open, Classified ·I.T.S. GmbH Autal 28 Lasnitzhohe Austria·Product code HRS·May 9, 2019

    SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 782118

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 1) 782150 2) 782106

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: (1) 782117 (2) 782143

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024

    Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/or spectra of the internal structure of the head, body or extremities, in any orientation. (REF) Numbers: 1) 782115 2) 782101 3) 782140

    FDA Recall
    Open, Classified ·Philips North America Llc·Product code LNH·September 3, 2024