Safety Alert for EVA TPN bags

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

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
    2012-04-23
  • 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
    Field safety notice: baxa eva tpn bags the food and drug administration (fda), united states, has issued a class ii recall on eva tpn bags, manufactured by baxa corporations inc.. the product is sold under three brand names: exacta mix eva bags, exacta mix dual-chamber eva halobag, and baxa calibration bags. the model numbers involved included the following: model 137, size 250 ml, cat. no. h938 137 3; model 138, size 500 ml, cat no. h938 138 3; model 139, size 1000 ml, cat no. h938 139 3; model 140, size 2000 ml, cat. no. h938 140 3; model 141, size 3000 ml, cat. no. h938 141 3; model 142, size 4000 ml, cat. no. h938 142 3; model 143, size 5000 ml, cat. no. h938 143 3; model 341, size 500/3000 ml, cat no. h938 341 3. the fda found that the spike port of eva tpn bags contains low levels of dehp which could leach out. current baxa product is mislabeled as non-dehp. according to the local supplier, the affected products have been distributed in hong kong. the local supplier is recalling the affected products. for details, please refer to fda website http://www.Fda.Gov/safety/recalls/enforcementreports/ucm300959.Htm if you are in possession of the product, please contact your supplier for necessary actions.

Device

  • Model / Serial
  • Product Description
    Medical Device Safety Alert: Baxa EVA TPN bags
  • Manufacturer

Manufacturer