Safety Alert for Premier Buffer A and B Reagent

According to Department of Health, this safety alert involved a device in Hong Kong that was produced by Trinity Biotech.

What is this?

Alerts provide important information and recommendations about products. Even though an alert has been issued, it does not necessarily mean a product is considered to be unsafe. Safety Alerts, addressed to health workers and users, may include recalls. They can be written by manufacturers, but also by health officials.

Learn more about the data here
  • Type of Event
    Safety alert
  • Date
    2017-02-28
  • Event Date Posted
    2017-02-28
  • Event Country
  • Event Source
    DH
  • Event Source URL
  • Notes / Alerts
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
  • Extra notes in the data
    Medical Device Safety Alert
  • Reason
    Medical device safety alert: trinity biotech premier buffer a and b reagent medical device manufacturer, trinity biotech, has issued a medical device safety alert concerning its premier buffer a reagent [product code (lot number): 01-03-0080 (6873, 6669)] and premier buffer b reagent [product code (lot number):: 01-03-0081 (6374), 01-03-0096 (6859, 6639, 6506), 42664 (6528, 6633 and 6526)]. the manufacturer has received reports of difficulty in recovering controls (qc verification), using the above reagent lots, following system activation or standby mode. upon review, the manufacturer has confirmed that the first two test results following system activation or standby mode, with these reagent lots, may result in a low bias, whether they are a control or patient sample. the manufacturer is asking users of the above listed reagent lots for testing to review the following scenarios: if two controls were run directly after activation or standby and met acceptable criteria, there is no action required. if initial controls failed but were re-run and met acceptable criteria, there is no action required. if only patient samples were run directly after activation or standby, then a review of the first two (2) patient sample results is required. affected users should also take the following actions- discontinue the use of the above reagent lots. destroy any remaining product. confirm end-users’ laboratory practice of the use of two controls (qc verification) immediately following system standby and system activations. according to the manufacturer, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 28 february 2017.

Device

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Trinity Biotech Premier Buffer A and B Reagent
  • Manufacturer

Manufacturer