BEUDAMED
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    DAAG MEDICAL INC

    FDA registration
    DAAG MEDICAL INC·1 product·🇺🇸 United States

    Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED OR OPENED. LATEX FREE, SINGLE USE Tyvek pouches, 10 per box, Smiths Medical ASD, Inc. Used to administer fluid and drugs intravenously.

    FDA Enforcement
    Class II ·Terminated·Smiths Medical Asd Inc·June 17, 2015

    Angio-Seal Vascular Closure Device. Ref 610109. 6F STS Platform. Sterilized by gamma radiation. For single use only. St. Jude Medical, Daig Division, Inc., Minnetonka, MN 55345-2126, USA.

    FDA Recall
    Terminated ·St. Jude Medical Daig Division·Product code MGB·August 22, 2005

    Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 Fr, 15 cm length Obturator supplied as a 10-pack box with 10 Individually packaged Obturators. Sterile EO. Single use. St. Jude medical, DAIG Division, Inc., Minnetonka, MN 55345-2126 USA

    FDA Recall
    Terminated ·St. Jude Medical Daig Division·Product code DYB·September 20, 2005

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST.JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·November 19, 2002

    HEMOSTATIC PUNCTURE CLOSURE DEVICE

    FDA Adverse Event
    Injury ·DAIG CORP. ST JUDE MEDICAL SC, INC., DAIG DIV.·Product code MGB·October 8, 1999

    Product consists of a syringe used to inject fluids during an angiographic procedure for fluoroscopic imaging. Labeling is as follows: Product Label ''***Argon Medical Device***REORDER NO./REF 193205***10cc Control Syringe FR/TR/FM w/ Reservoir***This device is designed for the administration and removal of fluids***DISPOSABLE***SINGLE USE ONLY***DO NOT RESTERILIZE***STERILE***EO***STERILIZED BY EtO***Sterile Unless Opened or Damaged***Argon Medical Devices, Inc. 1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669***'' Carton Label ''***Argon Medical Device***10cc Control Syringe FR/TR/FM w/ Reservoir***This device is designed for the administration and removal of fluids***REF/REORDER NO. 193205***Quantity: 25ea***STERILE***EO***STERILIZED BY EtO***DISPOSABLE***SINGLE USE ONLY***DO NOT RESTERILIZE***Sterile Unless Opened or Damaged***Argon Medical Devices, Inc. 1445 FLAT CREEK ROAD - ATHENS, TX 75751***800-927-4669***''

    FDA Recall
    Terminated ·Argon Medical Devices, Inc·Product code IZI·June 27, 2005

    Low Volume Extension Set, 72' w/Clamp FLL/MLL APV=1.3ml, STERILE, AND FLUID PATH NONPYROGENIC UNLESS PACKAGE IS DAMAGED OR OPENED. LATEX FREE, SINGLE USE Tyvek pouches, 10 per box, Smiths Medical ASD, Inc. Used to administer fluid and drugs intravenously.

    FDA Recall
    Terminated ·Smiths Medical Asd Inc·Product code FPA·May 4, 2015

    Deltec Cozmo 3 ml Insulin Cartridge with 0.7mm(22G) x 12.5mm (1/2 in.) needle and cap. Reorder No. 21-1750-24. Immediate container states STERILE EO, Rx Only , Deltec, Inc., St. Paul, MN 55112. Additional labeling states Cartridge is Sterile and nonpyrogenic unless package is opened or damaged. do not use if package is opened or damaged, or if product appears damaged. Made in Mexico for: Deltec 1265 Grey Fox Road, St. Paul, MN 55112 USA, Smiths, smiths Medical - a part of Smiths Group plc.

    FDA Recall
    Terminated ·Smiths Medical MD, Inc.·Product code LZG·October 15, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·March 26, 2004

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·March 12, 2004

    SPYGLASS ANGIOGRAPHIC CATHETER 4F, JL4, 100CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code DQO·March 9, 2004

    SPYGLASS ANGIOGRAPHIC CATHETER 4F PIG/155, 110CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code DQO·February 20, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·January 23, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·February 20, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·February 24, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·January 16, 2004

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·February 27, 2004

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·March 1, 2004

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, DAIG DIVISION, INC.·Product code MGB·March 18, 2004