BEUDAMED
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    Filters FDA Recall × Status: Terminated × Clear all

    AVANOS MIC-KEY SF Gastrostomy Feeding Tube

    FDA Recall
    Terminated ·Avanos Medical, Inc.·Product code KNT·July 29, 2020

    Fresenius 2008T Series Hemodialysis System

    FDA Recall
    Terminated ·Fresenius Medical Care Renal Therapies Group, LLC·Product code KDI·December 21, 2016

    Fresenius 2008K2 Series : Hemodialysis System

    FDA Recall
    Terminated ·Fresenius Medical Care Renal Therapies Group, LLC·Product code KDI·December 21, 2016

    Fresenius 2008K Series : Hemodialysis System

    FDA Recall
    Terminated ·Fresenius Medical Care Renal Therapies Group, LLC·Product code KDI·December 21, 2016

    Fresenius 2008K@home Series : Hemodialysis System

    FDA Recall
    Terminated ·Fresenius Medical Care Renal Therapies Group, LLC·Product code KDI·December 21, 2016

    ENNOVATE MIS REMOVALKEY SHORT, product code SZ380R

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code LXH·November 18, 2020

    Stryker Xia 3 Anti-Torque Key Manual Surgical Instrument; Catalog Number 48237026. Product Usage: : Reusable instrument used to aid in the final tightening of the spinal construct. Intended Use: The Anti-Torque Key allows the Torque Wrench to align with the tightening axis and maximizing the torque needed to lock the implant assembly during final tightening of the spinal construct.

    FDA Recall
    Terminated ·Stryker Spine·Product code NKB·January 12, 2012

    IMPAX 6.2.1 Network Gateway Server, License Key. Catalog # ABC code: EXEGE000. The product is used to transfer medical imaging data. AGFA Corp., Greenville, South Carolina 2960.

    FDA Recall
    Terminated ·AGFA Corp.·Product code LMD·December 11, 2007

    Picasso/Picasso Lite lasers Intended use: Dentistry.

    FDA Recall
    Terminated ·AMD Lasers, LLC·Product code GEX·April 15, 2010

    STOPCON Suction Valve-Suction Valve for GI-Endoscope DISTRIBUTED BY: KEY SURGICAL 8101 WALLACE ROAD / EDEN PRAIRIE, MN 55344 / USA Product Code: EN10232

    FDA Recall
    Terminated ·GA HEALTH COMPANY LIMITED Unit 18, 21/F Metropole Square; 2 On Yiu Street ,Shatin, N.T Shatin N.T. Hong Kong SAR·Product code OCX·November 3, 2020

    Xmatrx FISH (fluorescent in situ hybridization) Automated Staining System, Catalog number AS4010B

    FDA Recall
    Terminated ·Biogenex Laboratories·Product code KEY·January 24, 2008

    Xmatrx FISH (fluorescent in situ hybridization) Automated Staining System; Model Number/Catalog Number: AS4010B; The product is manufactured by: BioGenex Laboratories, Inc. 4600 Norris Canyon Road San Ramon, CA 94583 and Distributed by: Abbott Molecular, 1300 E. Touhy Ave - 2E, Des Plaines, IL 60018 Xmatrx Automated Staining System is intended for in vitro diagnostic use. It is suitable for fluorescent hybridization (FISH) applications.

    FDA Recall
    Terminated ·Biogenex Laboratories·Product code KEY·January 23, 2009

    Symphony Staining System (High Volume Stainer), KPA, Model Number 2200000, Ventana Medical Systems Inc

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code KEY·October 30, 2007

    VP 2000 Processor; an automated tissue stainer 100 volt - part 30-144100 or list 2J11-60; 117 volt - part 30-144101 or list 2J11-01, and part 30-102832 - processor only; 230 volt - part 30-144102 or list 2J11-04, and part 30-102833 processor only. Designed to automate and standardize slide specimen processing including deparafinization, FISH pretreatment and routine slide staining for the laboratory. The unit is preprogrammed to perform slide pretreatment protocols for FISH assays and can be programmed to perform routine histology/cytology slide staining or routine slide washing according to user requirements.

    FDA Recall
    Terminated ·Abbott Molecular·Product code KEY·September 15, 2008

    Ventana Medical System's Symphony Staining System, KPA, Model #: 2200000, Catalog #: 900-SYM1 & 900-SYM3, Ventana Medical Systems, Tucson, AZ

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code KEY·September 6, 2007

    Disetronic D-TRONplus Insulin Pump

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·July 24, 2003

    Stat Profile Critical Care Xpress (CCX and CCX+), CCX Creatinine Membrane Kit for CCX analyzer Catalog # 35238 Intended for in vitro diagnostic use by health care professionals and for point-of-care usage in the quantitative determination of pH, PCO2, PO2, SO2%, Hematocrit (Hct), Ca++, total hemoglobin (tHb), Oxyhemoglobin (O2Hb), Carboxyhemoglobin (COHb), Methemoglobin (MetHb), reduced hemoglobin (HHb), Oxygen content (O2Ct) and Oxygen capacity (O2Cap) in heparinized whole blood; Na+, K+, CL-; Ca++, Mg++, Glucose heparinized whole blood, serum, or plasma.

    FDA Recall
    Terminated ·Nova Biomedical Corporation·Product code CGL·August 11, 2008

    Vapofils with Stainless Steel Block Ends, Item Number V0507S (Sevofluane). The vapofil is a keyed anesthetic transfer tube that transfers the anesthetic from the bottle to the vaporizer.

    FDA Recall
    Terminated ·Southmedic Inc Po Box 1365 Barrie Canada Ontario·Product code CAD·April 21, 2006

    Posey Key Lock Belt (1334). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others..

    FDA Recall
    Terminated ·J T Posey Company·Product code FMQ·April 20, 2009

    Vapofils with Stainless Steel Block Ends, Item Number V0507F (Isoflurane). The vapofil is a keyed anesthetic transfer tube that transfers the anesthetic from the bottle to the vaporizer.

    FDA Recall
    Terminated ·Southmedic Inc Po Box 1365 Barrie Canada Ontario·Product code CAD·April 21, 2006