BEUDAMED
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    Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System

    FDA Recall
    Open, Classified ·Think Surgical, Inc.·Product code OLO·February 12, 2024

    AXIUM DETACHABLE COIL SYSTEM REF QC-4-12-HELIX; Axium Detachable Coil System REF QC-10-30-3D;

    FDA Recall
    Open, Classified ·Micro Therapeutics, Inc.·Product code HCG·April 27, 2022

    Alcon Custom Pak with Non-Latex Symbol, Pak: 12771-18, 18050-10, 18252-17, 12698-09, 15632-10, 3141-45, 12630-07, 18925-05, 19265-05, 13894-16, 17550-08, 12236-18, 11854-15, 8043-29, 12466-17, 15599-17, 14764-09, 13194-16, 17069-09

    FDA Recall
    Open, Classified ·Alcon Research LLC·Product code LRO·February 10, 2025

    NIM TRIVANTAGE EMG Endotracheal Tube

    FDA Recall
    Open, Classified ·Medtronic Xomed, Inc.·Product code ETN·December 22, 2021

    One Step P in vitro diagnostic test REF: 8194

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code JIR·April 2, 2026

    One Step pH in vitro diagnostic test REF: 31I4P

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code CEN·April 2, 2026

    ET III Nano-HA fixture System ET NH Dental Implant Model # ET3R5010B -Intended for Dental Implant Catalog #: AET3R5010B

    FDA Recall
    Open, Classified ·Hiossen Inc. Keystone Industrial Port Complex·Product code DZE·April 6, 2023

    QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code CHH·April 2, 2026

    Uric Acid in vitro diagnostic test REF: 31H0P

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code KNK·April 2, 2026

    One Step UTI in vitro diagnostic test REF: 3374

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code LJX·April 2, 2026

    MRI LED Mobile Exam Light Battery REF SL-111 This non-magnetic UL and CE approved battery is used in conjunction with SL-110, Mobile Exam Light

    FDA Recall
    Open, Classified ·MRIMed Inc.·Product code KZF·October 13, 2025

    TactiFlex Ablation Sensor Enabled Ablation Catheter, Models A-TFSE-FJ, 7.5 F shaft and an 8F distal section, Sterile.

    FDA Recall
    Open, Classified ·St. Jude Medical, Atrial Fibrillation Division, Inc.·Product code OAE·December 18, 2023

    One Step 10A in vitro diagnostic test

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code MVO·April 2, 2026

    One Step K in vitro diagnostic test REF: 81A4

    FDA Recall
    Open, Classified ·DFI Co., Ltd. 388-25 Gomo-Ro Jillye-Myeon Gimhae Korea (the Republic of)·Product code JIN·April 2, 2026

    Exactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE 38MM HUM LINER +2.5/ 320-42-00,145-DEG PE 42MM HUM LINER +0/ 320-42-03,145-DEG PE 42MM HUM LINER +2.5/

    FDA Recall
    Open, Classified ·Exactech, Inc.·Product code PHX·August 15, 2025

    Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only

    FDA Recall
    Open, Classified ·Micro Therapeutics, Inc.·Product code KRA·June 30, 2022

    Echelon -14, 45 Tip Shape, REF 145-5092150, sterile EO, Rx Only

    FDA Recall
    Open, Classified ·Micro Therapeutics, Inc.·Product code KRA·June 30, 2022

    Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG PE 38MM HUM LINER +2.5), REF:322-42-00 (145-DEG PE 42MM HUM LINER +0), REF: 322-42-03 (145-DEG PE 42MM HUM LINER +2.5)

    FDA Recall
    Open, Classified ·Exactech, Inc.·Product code PHX·August 15, 2025

    Innova IGS 630, Angiographic X-Ray, s5i system option used in generating fluoroscopic and rotational images of human anatomy for cardiovascular, vascular and non-vascular, diagnostic and interventional procedures.

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code IZI·March 15, 2019

    Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007 (Tempus Pro non-printer, IBP, with headset dock), 00-1024-R (Tempus Pro printer), 00-1026-R (Tempus Pro printer, IBP), 00-1007 [(Tempus Pro, BT Dock (IB Only)], 00-1004 00-1004 [Tempus Pro (IB Only)]

    FDA Recall
    Open, Classified ·Remote Diagnostic Technologies Ltd. Farnborough Aerospace Centre Aerospace Boulevard Farnborough United Kingdom·Product code MHX·April 16, 2025