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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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DISCOVERY (model nos. 1174, 1175, 1273, 1274 and 1275) pacemaker. Sterilized with gaseous ethylene ... 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
INTELIS II (model nos. 1349, 1384, 1385, 1483, 1484, 1485 and 1499) pacemaker. Sterilized with gas... 1 07/28/2005 Guidant Corporation
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
Baxter Colleague Triple Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
Baxter Colleague Single Channel Volumetric Infusion Pumps; Baxter Healthcare Corporation, Medication... 1 08/10/2005 Baxter Healthcare Corp.
Baxter Healthcare Corporation, Medication Delivery Division, Syndeo PCA Syringe Pump, product codes ... 2 08/16/2005 Baxter Healthcare Corp.
Accura System for Blood Filtration, product codes 5M5660 and ACCURA01 (international); a hemofiltrat... 2 08/18/2005 Baxter Healthcare Renal Div
Hemochron Jr. Whole Blood Microcoagulation system Low Range Activated Clotting Time. ACT-LR Cuvette... 3 08/23/2005 International Technidyne Corp.

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