Device Recall RECEPTAL CANISTER

  • Modèle / numéro de série
    *** DOMESTIC PRODUCT ***   List Numbers: 43449-04-11 and 43449-04-01;  Lot Numbers: All;   *** FOREIGN PRODUCT ***   List Numbers: 0L21297W1, 0L2129701, 0L2139701, 43449001L, 434490101, 434490102, 434490181, 434490181, 434490182, 4344901DX, 434496101, 434496161, 4344961A1, 434499090;  Lots: All
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) including the states of AL, AZ, CA, CO, FL, GA, IL, IN, KS, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NY, PA, SD, TX, UT, VA, and WA and countries of: Canada and EMEA.
  • Description du dispositif
    Product is labeled in part: LIST NO. 43449; RECEPTAL CANISTER; DO NOT FILL 900 ABOVE THIS LINE; Product of China; Hospira, Inc.,; Lake Forest, IL 60045 USA. || Used to isolate suction waste during surgeries, or to clear patient airways, throat or wounds to allow treatment.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Hospira Inc., 275 N Field Dr, Lake Forest IL 60045-2579
  • Société-mère du fabricant (2017)
  • Source
    USFDA