Orthopedic Systems Inc Doro Products Adapter, Product number 5979-300. The adaptor system is attached to OSI''s Spinal Frame, which is an operating room tabletop that is attached to a table base. The Frame is used to support patients during spinal surgery. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Doro Products Adapter, Product number 5979-300. The adaptor system is attached to OSI''s Spinal Frame, which is an operating room tabletop that is attached to a table base. The Frame is used to support patients during spinal surgery.
Brand
Orthopedic Systems Inc
Lot Codes / Batch Numbers
Product Number 5979-300, listing 878.4950.
Products Sold
Product Number 5979-300, listing 878.4950.
Orthopedic Systems Inc is recalling Doro Products Adapter, Product number 5979-300. The adaptor system is attached to OSI''s Spinal Fra due to Material used to manufacture accessory bracket does not meet product specification. The screw is normally composed of ''Torlon'', which is yellow. The. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Material used to manufacture accessory bracket does not meet product specification. The screw is normally composed of ''Torlon'', which is yellow. The part was made of "Tercite", which is blue.
Recommended Action
Per FDA guidance
A notification letter was sent to all 8 consignees on 02/16/2007. The firm will send service representatives to review any devices on site and replace with the proper part if needed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026