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.
데이터 추가 비고
Reamer - Product Code HTO
원인
It was reported that the ria drive shaft, tube assembly, and reamer head have the potential to break when incorrectly assembled or used improperly. precautionary statements are being added to the reamer / irrigator / aspirator (ria) surgical technique guide.
조치
DePuy Synthes sent an Urgent Medical Device Safety Notification dated May 28, 2015, to direct accounts and sales consultants to advise them of the patient risk associated with misassembly or misuse of the device.
Customers and sales force were instructed to remove the Surgical Technique Guide J4352 (all versions) dated 11/2011 or earlier and replace it with the updated Technique Guide (DSUS/TRM/0515/0620, Date 06/2015),and to return the completed verification response form.
If you have any further questions, please call (610) 719-5450. Thank you for your attention to this matter.
Nationwide Distribution and Internationally to Canada and Switzerland.
제품 설명
Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis