Recall of PAINSMART IOD (AMBULATORY INFUSION PUMP)

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by ZEVEX INC..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    20388
  • Event Risk Class
    I
  • Event Initiated Date
    2011-03-29
  • Event Country
  • Event Source
    HC
  • Notes / Alerts
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Extra notes in the data
  • Reason
    Accuracy of infusion with a syringe varies widely depending on the medication and stiction between the barrel and plunger of individual syringes. the effects of the variables have made the accuracy difficult to evaluate as each condition produces differing effects from the syringe variables. thereforezevex is not confident in providing accuracy percentages for syringes as they may be misleading if the application conditions are also considered. as a result the labeling will be modified to indicate the accuracy of delivery from a syringe cannot be guaranteed.

Device

  • Model / Serial
    Model Catalog: 360-1200 (Lot serial: Contact manufacturer.); Model Catalog: 360-1200 (Lot serial: >10 serial numbers.); Model Catalog: 360-1300P (Lot serial: Contact manufacturer.); Model Catalog: 360-1300 (Lot serial: Contact manufacturer.); Model Catalog: 360-1300P (Lot serial: >10 serial numbers.); Model Catalog: 360-1300 (Lot serial: >10 serial numbers.); Model Catalog: 360-1400 (Lot serial: Contact manufacturers.); Model Catalog: 360-1100 (Lot serial: Contact manufacturers.); Model Catalog: 360-1400 (Lot serial: >10 serial numbers.); Model Catalog: 360-1100 (Lot serial: >10 serial numbers.); Model Catalog: 350-1000 (Lot serial: >10 serial numbers.); Model Catalog: 350-1100 (Lot serial: >10 serial numbers.); Model Catalog: 350-1200 (Lot serial: >10 serial numbers.); Model Catalog: 350-1000 (Lot serial: Contact manufacturer.); Model Catalog: 350-1100 (Lot serial: Contact manufacturer.); Model Catalog: 350-1200 (Lot serial: Contact manufacturer.)
  • Product Description
    PAINSMART IOD (AMBULATORY INFUSION PUMP)
  • Manufacturer

Manufacturer

  • Manufacturer Address
    SALT LAKE CITY
  • Manufacturer Parent Company (2017)
  • Source
    HC