Medtronic Sofamor Danek USA Inc Medtronic Sofamor Danek, Prestige Cervical Disc System, Implant Trial, REF/Catalog #: 6972226, SIZE 6 X 12, MATL: Stainless Steel/Titanium, Rx only, Manufactured at: Bartlett, Tennessee USA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic Sofamor Danek, Prestige Cervical Disc System, Implant Trial, REF/Catalog #: 6972226, SIZE 6 X 12, MATL: Stainless Steel/Titanium, Rx only, Manufactured at: Bartlett, Tennessee USA
Brand
Medtronic Sofamor Danek USA Inc
Lot Codes / Batch Numbers
Lot Numbers: CN07G002, CN07F006, 434150, CN06M009, CN6M016, and 506850
Products Sold
Lot Numbers: CN07G002, CN07F006, 434150, CN06M009, CN6M016, and 506850
Medtronic Sofamor Danek USA Inc is recalling Medtronic Sofamor Danek, Prestige Cervical Disc System, Implant Trial, REF/Catalog #: 6972226, SIZE due to Implant mis-seating; Variance in size between the trial and the implant could cause the implant to be improperly seated.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Implant mis-seating; Variance in size between the trial and the implant could cause the implant to be improperly seated.
Recommended Action
Per FDA guidance
The firm notified their consignees of the problem and the recall by Urgent Medical Device Recall letter, telephone calls and electronic mail on 09/04/2007. Instructions include requests to immediately quarantine the product and hold for recalling firm collection.
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