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 manufacturer informed the recalling firm of a potential laser marking error in size identification on two columbus 4-in-1 femoral cutting guide instruments. the guides are correctly dimensioned, but the laser markings have been incorrectly etched.
조치
Both consignees were notified verbally on May 15, 2012 and asked to inspect their inventory for the recalled items, remove the mislabeled instruments and return them to the recalling firm. Both mislabeled instruments were returned to the firm. Customer questions were directed to (610) 984-9074.