Pascal Co Inc

Un dispositivo en la base de datos

  • Modelo / Serial
    the following 3 codes were recalled initially: (LOT EXP 110305, LOT EXP 110605, LOT EXP 110705) On October 3, 2005 the firm expanded the recall to include all product produced between October 2004 through August 2005. Following are all the recalled lot codes.  100105, 100205, 100305, 100405, 100505, 100605,  110105, 110205, 110305, 110405, 110505, 110605, 110705,  120105, 120205, 120305,  010106, 010206, 010306, 010406, 010506,  020106, 020206, 020306, 020406, 020506, 020606, 020706, 020806,  030106, 030206, 030306, 030406, 030506, 030606, 030706, 030806, 030906, 031006, 031106,  040106, 040206, 040306,  050106, 050206, 050306, 050406,  060106, 060206, 060306, 060406, 060506,  070106, 070206, 070306, 070406,  080106,
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    To dental product distributors nationwide and to 1 dental product distributor in Israel. Also directly to dental offices nationwide.
  • Descripción del producto
    product labeled in part: ''***banicide ADVANCED, A Reusable Sterilizing & Disinfecting Solution***Active Ingredient: Glutaraldehyde (1,5 Pentanedial) 3.5%***NET CONTENTS: 3.8l (ONE U.S. GALLON)***Manufactured by Pascal Company, Inc. 2929 N.E. Northup Way P.O. Box 1478 Bellevue, WA 98009-1478 USA***''