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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 110 of 500 Results *
Product: ivi Recall Date to: 07/05/2014
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Baxter System 1000 Single Patient Hemodialysis Systems, product codes SYS1000L3, SYS1000L3P, SYS1000... 2 08/24/2005 Baxter Healthcare Renal Div
Baxter Arena Hemodialysis Systems, product codes ARENADPX, ARENASP, ARENADPP, ARENASPX; Baxter Healt... 2 08/24/2005 Baxter Healthcare Renal Div
ITW Dymon Medaphene Plus Orange Disinfectant Spray, Pseudomonacidal, Virucidal, Mildewcidal, Fungici... 2 08/30/2005 ITW Dymon
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 09/23/2005 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, I.V. Syste... 1 09/23/2005 Baxter Healthcare Corp.
Guidant INSIGNIA I Ultra family of pacemakers includes the following: SR (models1190); and DR (mo... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I Plus family of pacemakers includes the following: SR (models1194); and DR (mod... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I AVT family of pacemakers includes the following: SSI (model 482), VDD (model 88... 2 09/24/2005 Guidant Corporation
Guidant INSIGNIA I Entra family of pacemakers includes the following: SSI (model numbers 0484 and 0... 2 09/24/2005 Guidant Corporation
Alto MSP (model 617) and Alto 2 MSP (model 627) Implantable cardioverter Defibrillator. Ventricular... 2 09/24/2005 ela Medical Llc

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