Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482
FDA device recall Z-0330-06 · posted 2005-12-28 · Terminated
Recall details
- Recalling firm
- Medtronic Sofamor Danek Instrument Manufacturing
- Reason for recall
- Screwdriver handle breakage
- Action taken
- The recalling firm sent out a letter dated 12/01/2005 explaining the problem and requesting return of the product.
- Root cause
- Other
- Status
- Terminated
- Product code
- HXX
- Quantity affected
- 75 units
- Distribution
- IL, IN, MI, CA, Japan, Netherlands
- Date initiated
- 2005-11-28
- Date posted
- 2005-12-28
- Date terminated
- 2006-11-09
- Location
- Bartlett, TN
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