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.
Depuy synthes is initiating a recall of certain lots of the craniomaxillofacial distraction system (ab distractor bodies and bc distractor bodies) because they may reverse post-operatively.
조치
The firm, DePuy Synthes, sent "Urgent Notice: Medical Device Recall" letters dated April 16, 2014 to affected customers. The letter identified the affected product, reason for recall, potential patient impact, mitigation steps for patients with distractors currently implanted and actions to be taken. Customers were instructed to review inventory, immediately remove the affected lots from stock, complete verification section of the letter and return the affected product.
For questions call 610-719-5450 or contact your DePuy Synthes Sales consultant.