BEUDAMED
    125 results · 30ms · Sources: EU EUDAMED, US FDA

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    Product 50 consists of all product under product code: JWH and same usage: Item no: 595002701 NEXGEN MIS TIBIA PLATE PR 595002702 NEXGEN MIS TIBIA PLATE PR 595003701 NEXGEN MIS TIBIA PLATE PR 595003702 NEXGEN MIS TIBIA PLATE PR 595003712 NEXGEN MIS TIBIA PLATE PR 595004701 NEXGEN MIS TIBIA PLATE PR 595004702 NEXGEN MIS TIBIA PLATE PR 595005701 NEXGEN MIS TIBIA PLATE PR 595005702 NEXGEN MIS TIBIA PLATE PR for use in total knee arthroplasty

    FDA Recall
    Terminated ·Product code JWH·January 11, 2016

    AIA-900 Analyzer, Part no. 022930, UDI 04560189283992

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code KHO·May 22, 2020

    VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical Lights)

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code KQM·June 4, 2024

    iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo Surgical Lights); e) 4068310 (Ceiling Trio Surgical Lights); f) 4068410 (Ceiling Quad Surgical Lights)

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code FTD·June 4, 2024

    Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)

    FDA Recall
    Open, Classified ·Baxter Healthcare Corporation·Product code FTD·June 4, 2024

    Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Epidural AnesthesiaTray. Product Catalog Numbers: 551879, 551994, 552024. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number: 332252. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix Continuous Epidural Anesthesia Tray. Product Catalog Numbers: 332075, 332266. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993, 552051, 552083, 552119, 555569. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

    FDA Recall
    Terminated ·B. Braun Medical, Inc.·Product code FMI·June 21, 2017

    Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments, DRILL GUIDES: a) REF 6975205, 5mm b) REF 6975206, 6mm c) REF 6975207, 7mm Product Usage: The PRESTIGE LP reusable instruments are intended for the surgical implantation of the PRESTIGE LP Cervical Disc. Medtronic reusable instruments must be sterilized prior to initial use and must be cleaned and sterilized prior to each re-use.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MJO·March 13, 2018

    Drill Tapered WP 5x11.5 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.

    FDA Recall
    Terminated ·Nobel Biocare Usa Llc·Product code DZI·March 14, 2019

    Drill Tapered WP 5x10 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.

    FDA Recall
    Terminated ·Nobel Biocare Usa Llc·Product code DZI·March 14, 2019

    Drill Tapered 6.0 6x8 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.

    FDA Recall
    Terminated ·Nobel Biocare Usa Llc·Product code DZI·March 14, 2019

    Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S. 3200TS Tourniquet Systems Model/Catalog Number: 60320010100 Software Version: Software version v2.06 or prior are within scope of the recall for A.T.S. 3200TS Product Description: A.T.S 3200TS Tourniquet Systems Component: N/A

    FDA Recall
    Open, Classified ·Zimmer Surgical Inc·Product code KCY·December 24, 2025