U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
The sterile battery may contain particulates within the sterile package.
조치
A customer notification letter was sent 12/23/15.
The letter instructs the customer to cease distribution and use of the recalled lots. It also recommends that the inventory and distribution records be evaluated immediately to ensure that affected product is removed from any potential point of use.
Return product to:
Returns Department (Recall complaint ClS-001)
Pro-Dex, Inc
2361 McGaw Avenue
Irvine, California 92614 USA
Reference the Recall Complaint # on the outside of the shipping box.
If any questions or concerns, please contact the
QARA group at Pro-Dex at 949 769 3200.