BEUDAMED
    43 results · 19ms · Sources: EU EUDAMED, US FDA

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    Pinook Micro Massager Distributed by www.pinookusa.com Used to strengthen the abdominal muscles.

    FDA Recall
    Terminated ·Pinook-Usa·Product code NGX·May 23, 2013

    Pinook Mini Massager Distributed by www.pinookusa.com. Used to strengthen the abdominal muscles.

    FDA Recall
    Terminated ·Pinook-Usa·Product code NGX·May 23, 2013

    IGFBP-3 Immunoradiometric Assay (IRMA) Kit, Part Number: DSL-6600 usage: The DSL6600 IGFBP-3 immunoradiometric assay (IRMA) kit provides materials for the quantitative measurement of IGFBP-3 in serum. This assay is intended for in vitro diagnostic use.

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code CFL·August 9, 2010

    Nichols Advantage Sample hGH Diluent Set (Catalog No. 62-7756)

    FDA Recall
    Terminated ·Nichols Institute Diagnostics·Product code CFL·May 2, 2005

    IG1, IGF-I reagent, Catalog # LKGF1; For the quantitative measurement of insulin-like growth factor I (IGF-I) in serum or heparinized plasma.

    FDA Recall
    Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CFL·April 15, 2016

    ST-AIA PACK HGH; Part Number: 025266 Assay, Metabolic

    FDA Recall
    Terminated ·Tosoh Bioscience Inc·Product code CFL·March 5, 2018

    IGFBP-3 ELISA Reagent Kit; Part Number" DSL-10-6600; Lot Numbers: 992743, 992287, 991916, 991530, 991432, 990220 & 890830 This assay is intended for in vitro diagnostic use.

    FDA Recall
    Terminated ·Beckman Coulter Inc.·Product code CFL·March 30, 2011

    Bausch & Lomb Boston Conditioning Solution, Original Formula, Bausch & Lomb Incorporated, Rochester, NY 14609. The product is packed in 1 fl oz (30 mL), 3 fl oz (90 mL), 3.5 fl oz (105 mL) and 4 fl oz (120 ml) bottles.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code MRC·October 30, 2009

    KY JELLY LUBRICANT 2 FL OZ, SKU 901443

    FDA Recall
    Open, Classified ·Family Dollar Stores, Llc.·Product code NUC·June 23, 2022

    NEW SKIN LIQUID BANDAGE CLEAR .3FL OZ, SKU 999417

    FDA Recall
    Open, Classified ·Family Dollar Stores, Llc.·Product code KMF·June 23, 2022

    Hot Ice, 1 fl. oz., Meta Labs LLC, UPC 80705-2 Product Usage: A topical gel that increases men and womens secual excitement and pleasure.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    Bausch & Lomb, Boston Conditioning Solution, Original Formula, For Rigid Gas Permeable Contact Lenses, 1 fl. oz. (30 ml), Bausch & Lomb Incorporated, Rochester, NY 14609.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code LPN·June 30, 2009

    Amo-O Herbal Stimulator, 2 fl. oz. Manufactured by Meta Labs, Alpharetta, GA 30076, UPC Code 80702-1 Product Usage: The product is a nonprescription, topical gel that is used to enhance libido and stimulate orgasmic pleasure.

    FDA Recall
    Open, Classified ·Altasource LLC dba Meta Labs LLC·Product code NA·February 3, 2014

    AQuify Drops, Long Lasting Comfort Drops * Relieves Dryness * For Soft and RGP Contact Lenses * 1/3 fl. Oz. (10mL) * Sterile * CIBA Vision Corp. Made In Canada Manufactured for: CIBA Vision Corporation, Duluth, GA 30097 USA

    FDA Recall
    Terminated ·Ciba Vision Corporation·Product code MRC·November 2, 2005

    Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical purposes to lubricate body orifices to facilitate entry of diagnostic or therapeutic devices. Single use only. Sterile if unopened, undamaged package.

    FDA Recall
    Terminated ·MEDLINE IND·Product code KMJ·December 12, 2016

    Bausch & Lomb, Renu Fresh Multi-purpose Solution, 2 fl oz (60 mL), Travel Kit, Manufactured by: Bausch & Lomb Place, Rochester, NY 14609 Daily cleaning, removing protein deposits, rinsing, chemical (not heat) disinfection, and storage of soft (hydrophilic) contact lenses.

    FDA Recall
    Terminated ·Bausch & Lomb Inc·Product code LYL·December 22, 2010

    X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012

    FDA Recall
    Terminated ·X-Cel X-Ray Corp·Product code KPR--·November 12, 2002

    IPS e.max ZirCAD CER/in. Prime A3 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth Article Number: 758439

    FDA Recall
    Open, Classified ·IVOCLAR VIVADENT AG BEDERSRASSE LIECHTSTEIN Germany·Product code EIH·April 5, 2024

    IPS e.max ZirCAD CER/in. Prime B1 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758441

    FDA Recall
    Open, Classified ·IVOCLAR VIVADENT AG BEDERSRASSE LIECHTSTEIN Germany·Product code EIH·April 5, 2024

    IPS e.max ZirCAD CER/in. Prime BL1 C17/3- A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758434

    FDA Recall
    Open, Classified ·IVOCLAR VIVADENT AG BEDERSRASSE LIECHTSTEIN Germany·Product code EIH·April 5, 2024