C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm
FDA device recall Z-0211-04 · posted 2003-12-11 · Terminated
Recall details
- Recalling firm
- Interpore Cross International Inc
- Reason for recall
- Step drills from Lot 25947 may have been mis-etched.
- Action taken
- The consignees will be notified by letter.
- Root cause
- Other
- Status
- Terminated
- Product code
- DKA
- Quantity affected
- 433 units
- Distribution
- U.S., Netherlands, Australia, Venezuela, Mexico, Columbia and Brazil
- Date initiated
- 2003-11-07
- Date posted
- 2003-12-11
- Date terminated
- 2004-04-20
- Location
- Irvine, CA
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