FDA Recall
Terminated
Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482
Recall: Z-0330-06
·
Initiated November 28, 2005
Recall
- Recall Number
- Z-0330-06
- Event Number
- 34196
- Firm
- Medtronic Sofamor Danek Instrument Manufacturing
- FEI Number
- 3004564008
- Product Code
- HXX
- Status
- Terminated
- Root Cause
- Other
- Initiated
- November 28, 2005
- Posted
- December 28, 2005
- Terminated
- November 9, 2006
- Address
- 2975 Brother Blvd, Bartlett, TN, 38133-3957
Description
Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482
Reason
Screwdriver handle breakage
Action
The recalling firm sent out a letter dated 12/01/2005 explaining the problem and requesting return of the product.
Distribution
IL, IN, MI, CA, Japan, Netherlands
Quantity
75 units