55715 articles — Page 162 of 2786
FDA recall notice for GE Healthcare, Seno Advantage 2.2 workstations with software version 22_01 and 22_02 A medical image review station that allows easy
FDA recall notice for GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume View CT Colonography/Navigator 2 software. (Version 4.0, 4.1,or 4
CPSC recall notice for Kitchen Selectives® 6-Speed Blender (Select Brands, of Lenexa, Kan.). Reason: The recalled products are Kitchen Selectives® 6-Speed Blend
CPSC recall notice for Kitchen table sets. Reason: This recall involves three-piece oak table and chair sets. Issued 2012-05-24.
FDA recall notice for LMA Esophageal Intubation Detector (EID), Catalog Number EID100 The device is used to assist verification of placement of the endotrach
FDA recall notice for Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX. "Instructions For Use" (QF7.5.1A.R01 thru QF7.5.1A.R06 Care and Hand
FDA recall notice for Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments are intended for use in
FDA recall notice for IntelliSpace Portal software and Extended Brillance Workspace software Intellispace Portal is a multimodality thin-client applications
CPSC recall notice for Portfolio 7-inch reflector assembly with glass lens. Reason: This recall involves circular, 7-inch diameter Portfolio aluminum reflector
CPSC recall notice for LED Clip-On Desk Lamps (He Shan Lide of China). Reason: This recall conducted by He Shan Lide involves pink and blue plastic LED desk l….
CPSC recall notice for Century Mattresses. Reason: This recall involves Chicago Century Furniture Corp. Issued 2012-05-23.
FDA recall notice for Pear juice concentrate 70 Brix in 55 gallon steel drums with plastic liner that are filled to 52 gallons. Labeled in part: "CLAREX PEAR J
FDA recall notice for Whole Oysters: 1) Empress Whole Oysters, NET WT 8 OZ. Distributed By Mitsui Foods Inc. Norwood NJ 07648 Product of Korea, UPC 7360000719.
FDA recall notice for BD GeneOhm Cdiff Assay , Catalog #441400 200, box tests 1-3 labeled in part***BD Diagnostics, 2555 boul, du Parc-Technologique, Quebec, QC
FDA recall notice for BD GeneOhm MRSA ACP Assay, Catalog #441639, box 200 tests labeled in part***GeneOhm Sciences Canada, Inc. 2555 Boul, du Parc-Technologique
FDA recall notice for Alere Triage Cardiac Panel PN 97000HS Used for the quantitative determination of creatine kinase MD (CK--MB), myoglobin and troponin I
FDA recall notice for BD GeneOhm VanR Assay , Catalog # 441250, 5 box tests labeled in part***GeneOhm Sciences Canada, Inc., 2555 boul, du Parc-Technologique,
FDA recall notice for Philips Digital Diagnost Software, software release 2.0.2 and 2.0.2SP1 including mirror icon Stationary Fluoroscopic system (Philips He
FDA recall notice for 4.5mm TI Multiloc Screw Length 28MM-Sterile Expiration: 04/29/2012 REF 04.019.028S Manufactured or Distributed by Synthes (USA) 1101
FDA recall notice for Triage D-dimer PN 98100 Used as an aid in the assessment and evaluation of patients suspected of having disseminated intravascular coag