BEUDAMED
    54 results · 29ms · Sources: EU EUDAMED, US FDA

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    EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism of 0.75 Diopters or less that does not interfere with visual acuity.

    FDA Recall
    Terminated ·Clerio Vision·Product code LPL·February 16, 2021

    Product is packed in a pouch which is labeled as MicroChoice FOOTSWITCH Linvatec LINVATEC CORPORATION LARGO, FL 33773 USA 5020-053

    FDA Recall
    Terminated ·Linvatec Corp DBA Linvatec/Hal·Product code HWE·January 24, 2003

    NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

    FDA Recall
    Open, Classified ·NOXBOX LTD·Product code MRN·September 9, 2025

    Cannulated graduated drill bit 1.9 mm diameter, with AO QC system, REF: INS-114 for use in orthopedic surgery.

    FDA Recall
    Terminated ·NEOSTEO 2 rue Robert Schuman Reze France·Product code HTW·November 3, 2020

    Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is manufactured and distributed by Maytex Corporation, CA Ear-loop face mask for basic medical/dental procedures.

    FDA Recall
    Terminated ·Maytex Corp·Product code FXX·May 15, 2013

    Clerio Vision, extreme H2O monthly, MED, DIA 14.0 PWR -2.25, UPC 675506803334 (6 count) and UPC 675506804478 (12 count) - Product Usage: for daily wear is indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism of 0.75 Diopters or less that does not interfere with visual acuity.

    FDA Recall
    Terminated ·Clerio Vision·Product code LPL·December 10, 2020

    COONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS FOR USE W/SIZE REGULAR ELBOW ELBOW COMP REPLACEMENT-REG SET STERILE PROD CLASS: 4100 OPERATION:9000 QTY/PKG:1 Product Usage: The ulnar and humeral components are connected by placing the hollow, outer axis pin across the two components and securing It with the solid Internal axis pin. The Inner and outer pin connection Is articulation point of the placement elbow.

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code JDC·November 19, 2012

    Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable Regular Humerals STERILE Rx, Tivanium QTY/PKG:1 Product Usage: The ulnar and humeral components are connected by placing the hollow, outer axis pin across the two components and securing It with the solid Internal axis pin. The Inner and outer pin connection Is articulation point of the placement elbow.

    FDA Recall
    Terminated ·Zimmer, Inc.·Product code JDC·November 19, 2012

    Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    DYONICS POWER Shaver Blades, 4.5mm Long Curved Full Radius Convex, package of 3. Catalog Number: 7205336 Product Usage: Smith & Nephew DYONICS Disposable Endoscopic Blades are indicated for resection of soft and osseous tissues in both large and small articular cavities.

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code HAB·May 6, 2011

    Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Li-ion Battery Housing for AR-400 DrillSaw Sports 400 System Product Usage: The battery housing is used to house the battery that powers the AR-400 DrillSaw Sports 400 device.

    FDA Recall
    Open, Classified ·Arthrex, Inc.·Product code HAB·August 27, 2018

    Biomet Stablecut Saw Blade - Reprocessed Sterile device -- Powered Saw and Accessories.

    FDA Recall
    Terminated ·Ascent Healthcare Solutions, Inc.·Product code HAB·March 11, 2008

    Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    DYONICS POWER Shaver Blades, 4.5mm Long Full Radius, package of 3 Catalog Number: 7205341 Product Usage: Smith & Nephew DYONICS Disposable Endoscopic Blades are indicated for resection of soft and osseous tissues in both large and small articular cavities.

    FDA Recall
    Terminated ·Smith & Nephew, Inc. Endoscopy Division·Product code HAB·May 6, 2011

    Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017

    Medical Device Exchange Wire (sternotomy wire); Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 046-072; 046-073; EXP (repackager), A & E Medical (OEM) Suture, nonabsorbable

    FDA Recall
    Terminated ·EXP Pharmaceutical Services Corp·Product code GAO·February 11, 2015

    Stryker Oscillating & Sagittal Blade - Reprocessed Sterile device -- Powered Saw and Accessories.

    FDA Recall
    Terminated ·Ascent Healthcare Solutions, Inc.·Product code HAB·March 11, 2008

    Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702

    FDA Recall
    Terminated ·Smith & Nephew, Inc.·Product code HAB·February 2, 2017