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    Emergency Products & Research, Inc.

    FDA registration
    Emergency Products & Research, Inc.·5 products·🇺🇸 United States

    KENDRICK

    FDA Adverse Event
    Malfunction ·EMERGENCY PRODUCTS AND RESEARCH·Product code IQF·July 2, 2008

    KENDRICK'S OTHER DEVICE FOR EXTRICATION

    FDA Adverse Event
    EMERGENCY PRODUCTS & RESEARCH·Product code IQF·August 13, 2008

    O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.

    FDA Recall
    Open, Classified ·Emergency Products & Research·Product code HSP·February 27, 2024

    O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.

    FDA Enforcement
    Class II ·Ongoing·Emergency Products & Research·April 3, 2024

    INFINION 16

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 11, 2023

    ZENITION

    FDA Adverse Event
    Malfunction ·PHILIPS INDIA LTD.·Product code OWB·July 19, 2024

    SPEAKMAN EYMEDIC SE-4270 SINGLE USE CONTAINER WATER, USP

    FDA Adverse Event
    Malfunction ·SPEAKMAN·Product code LWD·March 28, 2005

    MITRACLIP CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code NKM·July 31, 2020

    LTV1150 VENTILATOR

    FDA Adverse Event
    Injury ·PULMONETIC SSYTEMS CAREFUSION·Product code CBK·February 18, 2014

    LATEX EXAM GLOVES

    FDA Adverse Event
    Other ·ALLEGIANCE HEALTHCARE CORP·Product code LYY·April 11, 2000

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code NIQ·August 27, 2025

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·ABBOTT VASCULAR·Product code NIQ·August 27, 2025

    CaviCide, Part Numbers: 13-1025, 13-1000, 13-1024, MC-1000. Alternate brands: EnviroCide, part number: 13-3325. Private labeled products of Cavicide: Backscratchers Cavicide, part number: 13-4800. MaxiSpray Plus, part numbers: 13-7400 and 13-7405. pdCARE Surface Disinfectant, part numbers: 13-7525 and 13-7500. Z3 Surface Disinfectant, part number: 13-7900. CaviCide is a multi-purpose disinfectant/decontaminant cleaner for use on hard, non-porous inanimate surfaces. CaviCide is a bactericidal, virucidal, fungicidal, and tuberulocidal which is available in a ready-to-use, liquid form typically contained in 1 gallon bottles, 2.5 gallon bottles, 25 oz. spray bottles, or 55 gallon drums (depending on the item number). CaviCide may also be branded as a private label (see (1)(vi) below for names and Table 1 above for additional details). The product may be used (1) for precleaning non-instrument surfaces prior to disinfection; (2) for precleaning instruments prior to disinfection; (3) as a virucide on non-instrument surfaces; (4) as a disinfectant on non-instrument surfaces; (5) as a virucide on precleaned non-critical medical devices, instruments and implements; and (6) as a disinfectant on precleaned non-critical medical devices, instruments, and instruments. It is useful in health care settings such as hospitals, emergency medical settings, surgical centers, isolation areas, neonatal units, patient care areas, ophthalmic and optometric facilities, dental offices, dental operatories, animal care facilities, salon settings, emergency vehicles, schools, health club facilities, kitchens, bathrooms, prisons, morgues, and other critical care areas.

    FDA Enforcement
    Class II ·Terminated·Metrex Research, LLC.·September 5, 2012

    CALCITEK, INC.

    FDA Adverse Event
    Other ·CALCITEK, INC.·Product code DZE·December 30, 1996

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·August 3, 2017

    LTV 1150

    FDA Adverse Event
    Injury ·PULMONICS·Product code CBK·February 21, 2014

    EXPEDIUM SINGLE INNIE SET SCREW

    FDA Adverse Event
    Injury ·DEPUY RAYNHAM·Product code KWP·October 30, 2012

    JUVEDERM ULTRA PLUS XC TSK US

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·August 6, 2013

    MITRACLIP SYSTEM CLIP DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code NKM·April 28, 2020