CHESAPEAKE® Stabilization System 2008-90177Recalls & reported problems
VB Spine LLC · Expandable Drill Guide, Size 15 mm · Class 2
All models of CHESAPEAKE Stabilization System (31)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857181243), received between Mar 2, 2022 and Mar 2, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 2, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
A COMPANY REPRESENTATIVE REPORTED THAT THE CHESAPEAKE EXPANDABLE DRILL GUIDE DISENGAGED FROM THE IMPLANT DURING SURGERY WHILE THE SURGEON WAS PREPARING A PILOT HOLE FOR THE SECOND SCREW. THE DRILL GUIDE WAS NOT REATTACHED AND THE SECOND SCREW WAS INSERTED FREEHAND INTO THE PARTIALLY PREPARED HOLE. THE THIRD SCREW WAS NOT IMPLANTED. THE CHESAPEAKE ANTERIOR LUMBAR IMPLANT WAS PLACED WITH ONLY TWO OF THE THREE SCREWS SO THAT THE DEVICE WAS ONLY INSTRUMENTED TO A SINGLE ADJACENT VERTEBRAL BODY. THIS REPORT CAPTURES THE CHESAPEAKE EXPANDABLE DRILL GUIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13654447 ↗
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- Divergence® Anterior Cervical Fusion System G6626746Medtronic Sofamor Danek, Inc. · Intervertebral fusion device with integrated fixation, cervical21 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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