Abbott Spine SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine, SlimLine Hybrid, Corpectomy, ThinLine and Ant-Cer Anterior Cervical Plating Systems. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine, SlimLine Hybrid, Corpectomy, ThinLine and Ant-Cer Anterior Cervical Plating Systems.
Brand
Abbott Spine
Lot Codes / Batch Numbers
SC-AcuFix Core Instruments Surgical Techniques: Doc #499-0062-MKC, rev A.
Products Sold
SC-AcuFix Core Instruments Surgical Techniques: Doc #499-0062-MKC, rev A.
Abbott Spine is recalling SC-AcuFix Core Instruments Surgical Techniques covering SC-AcuFix SlimLine, SlimLine Hybrid, Corpect due to Modification to labeling for surgical implant.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Modification to labeling for surgical implant.
Recommended Action
Per FDA guidance
Firm contact of Sales Agencies by phone began on 11/11/05 to inform of changes to Surgical Techniques. Letter to surgeons using SC-AcuFix Systems as of 06/01/05 sent 11/14/05.
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