CHESAPEAKE Stabilization SystemRecalls & reported problems across all models
VB Spine LLC · 31 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 46
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls
- 1
We found 31 models of CHESAPEAKE Stabilization System by VB Spine LLC in the FDA's device registry (GUDID). Together they are named in 46 adverse event reports in the FDA's MAUDE database, received between Jan 11, 2016 and Jun 2, 2026 — classified as 1 injury, 45 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (16 reports).
1 FDA recall record name at least one of these models by its device identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
CHESAPEAKE Stabilization System recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Mar 16, 2021Terminated
Interference condition between the 10mm Drill Guide Inserter and the inner shaft that mates with the inserters. As a result, inner shafts do not mate flush with the collet inserters, and splaying of the collet. If implant falls into the spinal cord may cause a spinal cord injury or Incomplete seating of the inserter to the implant could result in misalignment of the screws with the inserter screw guide, potentially causing malposition of the screws into the adjacent vertebral bodies
Z-1410-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported CHESAPEAKE Stabilization System problems
Device problems
- Material Deformation16
- Fracture9
- Mechanical Problem9
- Difficult to Insert6
- Misassembled2
- Appropriate Device Problem Term/Code Not Available1
- Calibration Problem1
- Crack1
Patient problems
- No Clinical Signs, Symptoms or Conditions40
- No Information4
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
- Pain1
CHESAPEAKE Stabilization System models
31 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CHESAPEAKE Stabilization System 3608-90033Orthopedic manual surgical instrument1 recall0 reports
- CHESAPEAKE Stabilization System 2008-90025Orthopedic manual surgical instrument7 reports
- CHESAPEAKE Stabilization System 2008-90051Orthopedic manual surgical instrument5 reports
- CHESAPEAKE® Stabilization System 3601-13514Intervertebral fusion device with integrated fixation, cervical3 reports
- CHESAPEAKE® Stabilization System 2001-15530SPINAL VERTEBRAL BODY REPLACEMENT DEVICE2 reports
- CHESAPEAKE Stabilization System 2008-90029Orthopedic manual surgical instrument2 reports
- CHESAPEAKE® Stabilization System 2013-21530L10Intervertebral fusion device with integrated fixation, lumbar2 reports
- CHESAPEAKE Stabilization System 3608-90030Orthopedic manual surgical instrument2 reports
- CHESAPEAKE® Stabilization System 2001-15525SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 report
- CHESAPEAKE® Stabilization System 2008-90018Intervertebral fusion device with bone graft, cervical1 report
- CHESAPEAKE Stabilization System 2008-90019Orthopedic manual surgical instrument1 report
- CHESAPEAKE Stabilization System 2008-90028Orthopedic manual surgical instrument1 report
- CHESAPEAKE Stabilization System 2008-90030Orthopedic manual surgical instrument1 report
- CHESAPEAKE® Stabilization System 2008-90060Intervertebral fusion device with integrated fixation, lumbar1 report
- CHESAPEAKE® Stabilization System 2013-21130L5Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 2013-21136L15Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 2013-21340L15Intervertebral fusion device with integrated fixation, lumbar1 report
- CHESAPEAKE® Stabilization System 2013-21530L5Intervertebral fusion device with integrated fixation, lumbar1 report
- CHESAPEAKE® Stabilization System 3601-13516Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 3601-13814Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 3601-13816Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 3608-206123Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE® Stabilization System 3608-206123WIntervertebral fusion device with integrated fixation, lumbar1 report
- CHESAPEAKE® Stabilization System 3608-207133WIntervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE Stabilization System 3608-90008Orthopedic manual surgical instrument1 report
- CHESAPEAKE Stabilization System 3608-90029Orthopedic manual surgical instrument1 report
- CHESAPEAKE Stabilization System 3608-90031Orthopedic manual surgical instrument1 report
- CHESAPEAKE® Stabilization System 3608-90059Intervertebral fusion device with integrated fixation, cervical1 report
- CHESAPEAKE Stabilization System 3608-90075Orthopedic manual surgical instrument1 report
- CHESAPEAKE Stabilization System 3608-90080Orthopedic manual surgical instrument1 report
- CHESAPEAKE® Stabilization System 2008-90177Intervertebral fusion device with integrated fixation, cervical1 report
Recent CHESAPEAKE Stabilization System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CASCADIA UNIVERSAL DRILL FRACTURED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25365381 ↗MalfunctionFeb 25, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24448590 ↗MalfunctionJan 14, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CHESAPEAKE ANTERIOR LUMBAR UNIVERSAL DRILL DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24067509 ↗MalfunctionJan 9, 2026Mechanical Problem; Calibration Problem
A COMPANY REPRESENTATIVE REPORTED THAT A CASCADIA TORQUE LIMITING HANDLE WAS NOT "TORQUING OUT PROPERLY" AND WAS UNABLE TO FINAL TIGHTEN INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24023295 ↗MalfunctionJan 6, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23975097 ↗MalfunctionJan 6, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CHESAPEAKE ANTERIOR LUMBAR UNIVERSAL AWLS AND THE TIPS OF TWO CHESAPEAKE ANTERIOR LUMBAR UNIVERSAL DRILLS DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE FIRST OF TWO DRILLS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23975096 ↗MalfunctionJan 6, 2026Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23975094 ↗MalfunctionJan 6, 2026Material Deformation
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CHESAPEAKE ANTERIOR LUMBAR UNIVERSAL AWLS AND THE TIPS OF TWO CHESAPEAKE ANTERIOR LUMBAR UNIVERSAL DRILLS DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE SECOND OF TWO DRILLS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23975082 ↗MalfunctionDec 19, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23855433 ↗MalfunctionDec 19, 2025Material Deformation; Material Deformation
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23855432 ↗MalfunctionJul 17, 2025Fracture; Fracture
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22536064 ↗MalfunctionMar 11, 2025Difficult to Insert; Difficult to Insert
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21576995 ↗MalfunctionFeb 10, 2025Fracture; Fracture
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21349259 ↗MalfunctionSep 9, 2024Fracture; Fracture
IT WAS REPORTED THAT THE TIP OF A CHESAPEAKE AL UNIVERSAL DRILL FRACTURED OFF INTRA-OPERATIVELY. THE FRACTURED TIP WAS REMOVED FROM THE PATIENT AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH LESS THAN A ONE MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCES TO THE PATIENT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20176356 ↗MalfunctionSep 9, 2024Material Deformation; Material Deformation
IT WAS REPORTED THAT A CHESAPEAKE AL DRILL DEFORMED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCES TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20175567 ↗
Other VB Spine LLC products
- EVEREST Spinal System77 models · 336 reports · 3 recalls
- YUKON OCT Spinal System54 models · 238 reports · 3 recalls
- OZARK Cervical Plate System54 models · 270 reports
- MESA Spinal System55 models · 140 reports
- ALEUTIAN Interbody Systems37 models · 135 reports
- PYRENEES Cervical Plate System29 models · 96 reports
- DENALI Spinal System22 models · 80 reports
- CASCADIA Interbody System28 models · 65 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page