Interpore Cross International Inc C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm
Brand
Interpore Cross International Inc
Lot Codes / Batch Numbers
Lot #25947 Catalog # 1100-9019 & #1100-9020
Products Sold
Lot #25947 Catalog # 1100-9019 & #1100-9020
Interpore Cross International Inc is recalling C-Tek Anterior Cervical Plate System: 2.3mm/4.0mm Step Drill-14mm & 2.3mm/4.0mm Step Drill-16mm due to Step drills from Lot 25947 may have been mis-etched.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Step drills from Lot 25947 may have been mis-etched.
Recommended Action
Per FDA guidance
The consignees will be notified by letter.
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