BEUDAMED
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    ThromCat Thrombectomy Catheter System. 7F 2.5 -7.0 mm 150 cm. Catalogue number 63000-01. It is a single-use, disposable device that is used to perform percutaneous maceration and removal of thrombus and restoration of blood flow.

    FDA Recall
    Terminated ·Kensey Nash Corp·Product code MCW·February 7, 2007

    ThromCat Thrombectomy Catheter System. Catalog number 63000-01

    FDA Recall
    Terminated ·Kensey Nash Corp·Product code MCW·May 21, 2007

    Hill-Rom Affinity Four Birthing Bed, Model P3700B. Note: Not distributed in the U.S.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·November 21, 2007

    Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·May 28, 2021

    Hill-Rom Affinity Three Birthing Bed, Model P3700.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·August 18, 2006

    Hill-Rom Affinity Three Birthing Bed, Model P3700A.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·November 21, 2007

    Affinity Four Birthing Bed P3700 Product Usage: The Affinity, Four Birthing Bed is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery ) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market. They are not intended for use as general hospital beds.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·April 2, 2012

    Hill-Rom brand Affinity three birthing bed

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·April 24, 2003

    Hill-Rom brand Century+ series bed

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·April 24, 2003

    Hill-Rom Affinity Birthing Bed, Model P3600.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·November 21, 2007

    Affinity Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·June 26, 2014

    Hill-Rom Affinity Two Birthing Bed, Model P3600.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·November 21, 2007

    Affinity Four Birthing Bed Model P3700 The primary packaging is pictured below, and utilizes a metal packing brace, standard corrugated cardboard and plastic banding. When possible these beds are shipped as a quantity of two (2) together as shown with the nylon strapping. These are shipped in standard freight containers. There is no secondary packaging.

    FDA Recall
    Terminated ·Hill-Rom, Inc.·Product code KNC·July 15, 2016

    VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

    FDA Enforcement
    Class II ·Terminated·Greiner Bio-One North America, Inc.·April 22, 2020

    The VITEK¿ 2 Anaerobic and Corynebacteria identification card (ANC) is intended for use with the VITEK¿ 2 Systems for the automated identification of most clinically significant anaerobic organisms and Corynebatcerium species. The VITEK¿ 2 ANC identification card is a single-use disposable. A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.

    FDA Enforcement
    Class II ·Terminated·BioMerieux SA·June 20, 2018

    VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

    FDA Recall
    Terminated ·Greiner Bio-One North America, Inc.·Product code GIM·March 12, 2020

    VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged - Product Usage: indicated for use in collection and transport of venous whole blood for coagulation testing.

    FDA Enforcement
    Class II ·Terminated·Greiner Bio-One North America, Inc.·May 12, 2021

    BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes, 4.5 mL, 13 x 75 mm, Mfd: Becton Dickinson and Company Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection Tube that provides means of collecting, transporting and processing blood in a closed tube. The buffered sodium citrate additive provides an anti-coagulated specimen that may be used for clinical laboratory coagulation assays and determinations.

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code JKA·March 16, 2017

    EM2+A NC AEM Monotor (NON-COM)

    FDA Recall
    Terminated ·Encision, Inc.·Product code GEI·June 23, 2003

    Greiner bio-one, VACUETTE TUBE, 9NC Coagulation Citrate 3.2%, 3.5ml blue cap-black ring, 24 racks of 50, 1200 pcs in total, non ridged, sandwich tube, Ref: 454332, Lot B040404, Expiry 2005-04, Sterile.

    FDA Recall
    Terminated ·Greiner VACUETTE North America·Product code GIM·July 27, 2004