BEUDAMED
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    AxSYM CMV IgG Reagent Pack; list 04B47; 100 test pack; in-vitro diagnostic; Abbott Laboratories, Abbott Park, IL 60064

    FDA Recall
    Terminated ·Abbott Laboratories·Product code LFZ·April 23, 2007

    Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured by Zeus Scientific, Inc., Raritan, NJ.

    FDA Recall
    Terminated ·Zeus Scientific Inc·Product code LFZ·June 12, 2003

    Diamedix Is-CMV IgG Test Kit

    FDA Recall
    Terminated ·Diamedix Corporation·Product code LFZ·March 26, 2015

    VIDAS 3 software v. 1.1.4

    FDA Recall
    Terminated ·BioMerieux SA Chemin De L'Orme Marcy L'Etoile France·Product code LFZ·January 11, 2017

    VIDAS CMV IgG Assay

    FDA Recall
    Terminated ·bioMerieux·Product code LFZ·June 9, 2004

    Premier CMV IgG Elisa Kits, EIA diagnostic test kits, 96 tests per kit, Catalog Numbers: 620096 and 9Z9501G.

    FDA Recall
    Terminated ·Meridian Bioscience Inc·Product code LFZ·June 18, 2003

    AxSYM CMV IgG Reagent Pack; Abbott Laboratories, Abbott Park, IL 60064; The AxSYM CMV IgG assay is a Microparticle Enzyme Immunoassay (MEIA) for the semi-quantitative measurement of IgG antibodies to cytomegalovirus in human serum and plasma (EDTA, heparin or sodium citrate) as an indication of past or current infection with cytomegalovirus; list 4B47-20

    FDA Recall
    Terminated ·Abbott Laboratories·Product code LFZ·January 19, 2009

    CHS Custom Convenience Kit- COBAN¿, LF (1"X5 YDS) Product Number:D5-14591

    FDA Enforcement
    Class II ·Terminated·Custom Healthcare Systems, Inc.·October 31, 2018

    Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Enforcement
    Class II ·Terminated·Andover Healthcare Inc.·October 30, 2019

    Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap

    FDA Enforcement
    Class II ·Terminated·Andover Healthcare Inc.·October 30, 2019

    CHS Custom Convenience Kit- COBAN, LF (1"X5 YDS) Product Number:D5-14591

    FDA Recall
    Terminated ·Custom Healthcare Systems, Inc.·Product code LRO·August 13, 2018

    OsteoPack 3 FZ 22cc. Product is labeled in part: ''***Processed at: Regeneration TECHNOLOGIES, INC. Alachua, Florida USA***SINGLE PATIENT USE ONLY***''.

    FDA Recall
    Terminated ·Regeneration Technologies, Inc.·Product code MQV·October 14, 2005

    WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of steam Soft touch facial & nasal masks" Product labeling reads in part: "Well at Walgreens***WARM Helps relieve symptoms of stuffy nasal passages, congestion or scratchy throats due to cold, flu or allergies

    FDA Recall
    Terminated ·Bigwall Enterprises·Product code KFZ·November 20, 2015

    Weck, Bipolar Forceps Cord, REF 394236, 1 (One) Cord, Length 12 Feet (3.7m), Sterile, Single Use, Disposable, Weck Closure Systems, Distributed by : Weck Closure Systems, One Weck Dr. Research Triangle Park, NC 27709, USA

    FDA Recall
    Terminated ·Product code FFZ·January 25, 2001

    Vicks brand Warm Mist Humidifier, Model V610, ''Pure Warm Moisturizer for Soothing Relief of Cold and Flu Symptoms'' sold over the counter. Firm on the label: Distributed by Kaz Inc., under license from the Procter & Gamble Company, Cincinnati, OH 45202. UPC code 3 28785 20610 4.

    FDA Recall
    Terminated ·Product code KFZ·April 15, 2003