BEUDAMED
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    ROCHE DISETRONIC MEDICAL SYSTEMS AG

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS, INC·Product code FPA·April 4, 2006

    H-TRON V-100 INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·March 17, 1998

    Disetronic brand 3.15 ml glass cartridges used with H-tron, H-tron plus, Panomat C, Panomat P, Panomat T, Panomat V and Dahedi Infusion pumps and Pen 10 insulin pens, 1 cartridge; manufactured by Disetronic Medical Systems AG, CH-3401, Burgdorf, Switzerland; catalog number 150.0042.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004

    Disetronic brand 3.15 ml glass cartridges used with H-tron, H-tron plus, Panomat C, Panomat P, Panomat T, Panomat V and Dahedi Infusion pumps and Pen 10 insulin pens, 1 cartridge; manufactured for Disetronic Medical Systems AG. CJ-3401, Burgdorf, Switzerland; catalog number 150.0272.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004

    Disetronic brand 3.15 ml glass cartridges used with H-tron, H-tron plus, Panomat C, Panomat P, Panomat T, Panomat V and Dahedi Infusion pumps and Pen 10 insulin pens in box of 25; manufactured for Disetronic Medical Systems AG, CH-3401, Burgdorf, Switzerland; catalog number 3001061.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004

    Disetronic brand 3.15 ml glass cartridges used with H-tron, H-tron plus, Panomat C, Panomat P, Panomat T, Panomat V and Dahedi Infusion pumps and Pen 10 insulin pens in box of 25 cartridges, 25 needles; manufactured by Disetronic Medical Systems AG, CH-3401, Burgdorf, Switzerland; catalog number 300.0419.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004

    Disetronic brand 3.15 ml glass cartridges used with H-tron, H-tron plus, Panomat C, Panomat P, Panomat T, Panomat V and Dahedi Infusion pumps and Pen 10 insulin pens in 10 x 10 box (10 cartidges per blister pack; 10 blister packs per box; Manufactured by Disetronic Medical Systems AG, CH-3401, Burgdorf, Switzerland; catalog number 150.0157.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code LZG·May 17, 2004

    H-TRONPULS V100 INSULIN INFUSION PUMP

    FDA Adverse Event
    Death ·DISETRONIC MEDICAL SYSTEMS AG·Product code LZG·June 28, 2000

    SPIRIT INSULIN PUMP

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS AG·Product code LZG·August 12, 2023

    MULTIFUSE PUMP

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS AG·Product code FRN·July 2, 1999

    DISETRONIC H-TRON V 100

    FDA Adverse Event
    Death ·DISETRONIC MEDICAL SYSTEMS AG·Product code LZG·February 6, 1998

    DISETRONIC ULTRAFLEX

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEM AG·Product code FOZ·March 11, 2007