Events

Field Safety Notices about Suction system, receptal

According to Swiss Agency for Therapeutic Products, this field safety notices involved a device in Switzerland that was produced by Hospira (Dominican Republic).

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event ID
    Vk_20100624_04
  • Event Date Posted
    2010-07-12
  • Event Country
    Switzerland
  • Event Source
    SATP
  • Event Source URL
    https://fsca.swissmedic.ch/mep/#?q=Vk_20100624_04
  • Notes / Alerts
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Switzerland.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • Extra notes in the data

Device

Suction system, receptal
  • Model / Serial
    OL2129701 Receptal 1L PVC Liner OL21297W1 Receptal 1L PVC Liner OF8079701 Receptal 1.5L PVC Liner OG6619701 Receptal 2L PVC Liner OG9159701 Receptal 2L PVC Liner OE0989701 Receptal 2L PVC Liner OF8069701 Receptal 2L P
  • Product Description
    MD: Suction system canister liner
  • Manufacturer
    Hospira (Dominican Republic)

Manufacturer

Hospira (Dominican Republic)
  • Manufacturer Parent Company (2017)
    Pfizer
  • Source
    SATP