Events

translation missing: en.activerecord.attributes.event.titles.recall_field_safety_notice

According to Saudi Food & Drug Authority, this translation missing: en.activerecord.attributes.event.types.recall_field_safety_notice involved a device in Saudi Arabia that was produced by Arrow International Inc.

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
    Recall / Field Safety Notice
  • Event ID
    mdprc 039 08 15 000
  • Event Initiated Date
    2015-08-12
  • Event Country
    Saudi Arabia
  • Event Source
    SFDA
  • Event Source URL
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=4&rid=7984
  • Notes / Alerts
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug Authority, 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 Saudi Arabia.
  • Extra notes in the data
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Reason
    Arrow is recalling certain lots of the products referenced above due to the possibility that the catheter peel-away component hub tabs may prematurely detach when the practitioner begins to peel apart the sheath body from the catheter.

Device

ARROW® International PICC Kits with Peel-Away Sheath Component
  • Model / Serial
    Products : ASK‐02041‐SEH1, CA‐05052‐HP, CDC‐34052‐VPS, EU‐05552‐HPMSB, ASK‐04001‐DU4, CA‐05052‐HPX, CDC‐35041‐VPS, FR‐04041, ASK‐04052‐AC, CDC‐02041‐MK1A, CDC‐35052‐VPS, FR‐04041‐CF, ASK‐05041‐LM4, CDC‐04041‐HPK1A, CDC‐35541‐VPS, FR‐05041, ASK‐05052‐SFL, CDC‐04052‐HPK1A, CDC‐35552‐VPS, FR‐05041‐CF, ASK‐05541‐MS2, CDC‐05041‐HPK1A, EU‐04041‐HP, FR‐05541‐CF, ASK‐05541‐MS3, CDC‐05052‐HPK1A, EU‐04041‐HPMSB, PI‐01451‐LS, ASK‐15552‐LM2, CDC‐05541‐HPK1A, EU‐04052‐HPMSB, PI‐01451‐LS5, ASK‐15552‐MS3, CDC‐05542‐PK1A, EU‐05041‐HPMSB, PK‐01451‐WS, ASK‐35041‐JHVA, CDC‐05552‐HPK1A, EU‐05052‐HPMSB, PK‐01451‐WSSP, CA‐05041‐HP, CDC‐15552‐HPK1A, EU‐05541‐HP, UK‐05041‐HPMIN, CA‐05041‐HPX, CDC‐34041‐VPS, EU‐05541‐HPMSB Lot Numbers: Refer to Appendix 2
  • Product Description
    catheter peel-away component
  • Manufacturer
    Arrow International Inc

Manufacturer

Arrow International Inc
  • Manufacturer Parent Company (2017)
    Teleflex Incorporated
  • Manufacturers representative
    Gulf Medical Co.
  • Source
    SFDA