Recall: Fresenius Actuator Boards for Series 2008

The FDA has announced that the previous recall of Fresenius Series 2008 HD/HHD machines (https://nwrnbulletins.wordpress.com/2014/01/17/recall-fresenius-series-2008-hdhhd-machines/) has been amended to include “Revision K” Actuator Test Boards sold as replacement parts.  For a list of serial numbers affected, see http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1618-2014&w=05212014&lang=eng.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s