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U.S. Department of Health and Human Services

Medical Device Recalls
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91 to 100 of 500 Results *
Product: ivi Recall Date to: 07/05/2014
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Product Description
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Recall
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Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 01/31/2006 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 01/31/2006 Baxter Healthcare Corp.
Baxter Meridian Hemodialysis Instrument, product codes 5M5576 and 5M5576R; Baxter Healthcare Corpora... 1 12/14/2005 Baxter Healthcare Renal Div
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.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
CONTAK TR (Model no. 1241) pacemaker. Sterilized with gaseous ethylene oxide. Guidant Corporatio... 1 07/28/2005 Guidant Corporation
DISCOVERY II (model nos. 481, 981 1184, 1186, 1187, 1283, 1284, 1285 and 1286) pacemaker. Steriliz... 1 07/28/2005 Guidant Corporation
MERIDIAN (model nos. 476, 976, 1176 and 1276) pacemaker. Sterilized with gaseous ethylene oxide. ... 1 07/28/2005 Guidant Corporation

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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