Safety Alert for Premier Buffer 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
    2017-06-07
  • Event Date Posted
    2017-06-07
  • 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 b reagent medical device manufacturer, trinity biotech, has issued a medical device safety alert concerning its premier buffer b reagent [product code: 01-03-0096 (940 ml); lot number: 6524]. the manufacturer has identified that the closed bottle stability for some bottles of lot 6524 may be reduced due to a broken seal under the cap of unopened bottles. in cases where a broken seal of an unopened bottle is encountered, the open bottle stability is essentially started and the bottle stability performance will be reduced, as it would over time when installed on the premier hb9210 system. where analytical run qc recovery is within range, the performance of the system and results are acceptable. however, if an unopened reagent bottle is found to have a broken seal prior to use, the open bottle stability has started. prior to consumption of the bottle, it may be observed that controls drift out quicker than normal, thereby requiring more frequent calibrations. the qc recovery (controls) verification will identify and contain this issue, as designed and there is no need for review of previously reported results. a thorough investigation into the root cause has been conducted and no other lots are affected. to avoid need for extra control runs and calibrations, the manufacturer recommends: discontinue the use of the above reagent lots. destroy any remaining product. notify all end-users of this notification. product replacement is on-going. according to the local supplier, 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 7 june 2017.

Device

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

Manufacturer