BEUDAMED
    72 results · 22ms · Sources: EU EUDAMED, US FDA

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    Medline Convenience kits labeled as: 1) OR CLEAN UP KIT, Pack Number DYK1002355X3, 2) CLEANING & CUTTING, Pack Number DYNJ84657

    FDA Recall
    Open, Classified ·MEDLINE INDUSTRIES, LP Northfield·Product code OKG·April 8, 2024

    BostonSight SCLERAL Lens

    FDA Recall
    Open, Classified ·Boston Foundation For Sight·Product code HQD·June 10, 2025

    BostonSight PROSE Lens.

    FDA Recall
    Open, Classified ·Boston Foundation For Sight·Product code HQD·June 10, 2025

    Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)

    FDA Recall
    Open, Classified ·Philips Healthcare·Product code OWB·September 24, 2021

    SenTec Digital Monitor, Model SDM, is a portable stand-alone patient monitor indicated for continuous, noninvasive patient monitoring of carbon dioxide partial pressure (PCo2), oxygen partial pressure (POs), functional oxygen saturation (PsO2), and pulse rate (PR), using either a single digital sensor (V-Sign Sensor 2 or OxiVenT sensor).

    FDA Recall
    Open, Classified ·SenTec AG Ringstrasse 39 Therwil Switzerland·Product code LKD·December 10, 2020

    Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software

    FDA Recall
    Open, Classified ·Abbott Medical·Product code PNJ·May 12, 2026

    Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.

    FDA Recall
    Open, Classified ·Maquet Cardiopulmonary Gmbh Kehler Str. 31 Rastatt Germany·Product code KRI·June 27, 2025

    2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code ERA·May 9, 2025

    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

    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

    Permobil TiLite, Models: Aero Z, and ZRA

    FDA Recall
    Open, Classified ·TiSport, Llc·Product code IOR·September 24, 2021

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

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

    DePuy Synthes Hammertoe Continuous Compression Implants, Product No. 46.239.001

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

    SPEED 9X10X10mm Continuous Compression Implant, Product No. SE-0910

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

    SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit, Product No. SE-2020-10. Used with DePuy Synthes SPEEDSHIFT Continuous Compression Staple Implants for bone fixation and management of fracture and reconstructive surgery.

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

    Osteosynthesis Compression Staple EasyClip

    FDA Recall
    Open, Classified ·Stryker GmbH Bohnackerweg 1 Selzach Switzerland·Product code JDR·September 25, 2020

    Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)

    FDA Recall
    Open, Classified ·D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands·Product code HQC·January 15, 2024

    Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)

    FDA Recall
    Open, Classified ·D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands·Product code HQC·January 15, 2024

    Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

    FDA Recall
    Open, Classified ·D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Scheijdelveweg 2 Zuidland Netherlands·Product code HQC·January 15, 2024

    Merlin PCS 3650 programmer Model 3330 software

    FDA Recall
    Open, Classified ·St. Jude Medical, Cardiac Rhythm Management Division·Product code OSR·March 10, 2022