CASCADIA Interbody SystemRecalls & reported problems across all models
VB Spine LLC · 28 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 65
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls
- 0
We found 28 models of CASCADIA Interbody System by VB Spine LLC in the FDA's device registry (GUDID). Together they are named in 65 adverse event reports in the FDA's MAUDE database, received between Oct 23, 2018 and Sep 21, 2026 — classified as 5 injuries, 60 malfunctions.
The most frequently reported specific device problem is “Fracture” (36 reports).
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
Most reported CASCADIA Interbody System problems
Device problems
- Fracture36
- Mechanical Jam10
- Mechanical Problem6
- Insufficient Device Problem Information5
- Material Deformation5
- Adverse Event Without Identified Device or Use Problem3
- Difficult to Insert3
- Migration3
Patient problems
- No Clinical Signs, Symptoms or Conditions59
- Pain3
- Cerebrospinal Fluid Leakage1
- Cyst(s)1
- Nerve Damage1
- No Consequences Or Impact To Patient1
CASCADIA Interbody System models
28 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CASCADIA™ Interbody System 6101-90167Intervertebral fusion device with bone graft, lumbar24 reports
- CASCADIA™ Interbody System 7902-90033Intervertebral fusion device with bone graft, cervical7 reports
- CASCADIA™ Interbody System 6101-90164Intervertebral fusion device with bone graft, lumbar4 reports
- CASCADIA™ Interbody System 6101-2103209TL7-G2Intervertebral fusion device with bone graft, lumbar2 reports
- CASCADIA™ Interbody System 6101-2103211TL7-G2Intervertebral fusion device with bone graft, lumbar2 reports
- CASCADIA™ Interbody System 7908-42F223Intervertebral fusion device with bone graft, lumbar2 reports
- CASCADIA™ Interbody System 7902-90102Intervertebral fusion device with integrated fixation, lumbar2 reports
- CASCADIA™ Interbody System PRO-1076-02Intervertebral fusion device with bone graft, lumbar2 reports
- CASCADIA™ Interbody System 6101-2102808TL7-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2102812TL7-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2102814NC-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2103208TL7-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2185010LL8-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-2185012LL8-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-2225510LL8-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2225512LL8-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2131607CL7-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-90170Orthopedic manual surgical instrument1 report
- CASCADIA™ Interbody System 6101-2123613TL7-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-2102808NT6-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-2102810NT6-G2Intervertebral fusion device with bone graft, cervical1 report
- CASCADIA™ Interbody System 6101-2852806NL12-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2852808NL12-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 6101-2852810NL12-G2Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System 7908-42F183Intervertebral fusion device with integrated fixation, lumbar1 report
- CASCADIA™ Interbody System 7908-41F24LIntervertebral fusion device with integrated fixation, lumbar1 report
- CASCADIA™ Interbody System SP-4153Intervertebral fusion device with bone graft, lumbar1 report
- CASCADIA™ Interbody System PRO-1076-01Intervertebral fusion device with bone graft, lumbar1 report
Recent CASCADIA Interbody System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50849148 ↗MalfunctionAug 7, 2026Fracture; Difficult to Remove
A health professional reported that the tip of a Cascadia AN Lordotic-Oblique Inserter fractured intra-operatively and was difficult to disassemble from an interbody. The procedure was completed successfully with a 15 minute surgical delay. No adverse consequences were reported. Inspection of additional returned products indicates that the tip of a second Cascadia Lordotic Oblique Inserter fractured and was difficult to disassemble from an interbody, and that the threading of one Cascadia Lordotic-Oblique Interbody was deformed. This report captures the second fractured Inserter.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50182169 ↗MalfunctionJul 21, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25898436 ↗MalfunctionJun 25, 2026Fracture; Difficult to Remove
A HEALTH PROFESSIONAL REPORTED THAT THE TIP OF A CASCADIA AN LORDOTIC-OBLIQUE INSERTER FRACTURED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY. NO ADVERSE CONSEQUENCES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25630912 ↗MalfunctionJun 24, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CASCADIA AN LORDOTIC-OBLIQUE INSERTER FRACTURED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED WITH NO SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25615620 ↗InjuryJun 11, 2026Insufficient Device Problem Information
MalfunctionMay 20, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS FRACTURED 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 INSERTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25233698 ↗MalfunctionMay 20, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS FRACTURED 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 INSERTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25233686 ↗MalfunctionMar 19, 2026Fracture
IT WAS REPORTED THAT THE TIP OF A CASCADIA LORDOTIC OBLIQUE INSERTER FRACTURED OFF INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 1-MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24643732 ↗MalfunctionFeb 26, 2026Mechanical Problem; Inaccurate Information
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24464787 ↗MalfunctionFeb 16, 2026Fracture
IT WAS REPORTED THAT ONE OF THE LATERAL PRONGS FROM TWO CASCADIA LORDOTIC OBLIQUE INSERTERS FRACTURED OFF 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 CASCADIA LORDOTIC OBLIQUE INSERTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24348450 ↗MalfunctionJan 27, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIP OF A CASCADIA AN LORDOTIC-OBLIQUE INSERTER FRACTURED INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 5 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24188924 ↗MalfunctionDec 23, 2025Inadequacy of Device Shape and/or Size; Use of Device Problem; Inadequacy of Device Shape and/or Size; Use of Device Problem
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23882174 ↗MalfunctionDec 17, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS FRACTURED OFF INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE FIRST OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23827585 ↗MalfunctionDec 17, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE TIPS OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS FRACTURED OFF INTRA-OPERATIVELY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH A 15 MINUTE SURGICAL DELAY AND NO ADVERSE CONSEQUENCE TO THE PATIENT. THIS REPORT CAPTURES THE SECOND OF TWO CASCADIA AN LORDOTIC-OBLIQUE INSERTERS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23827572 ↗
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
- CHESAPEAKE Stabilization System31 models · 46 reports · 1 recall
- PYRENEES Cervical Plate System29 models · 96 reports
- DENALI Spinal System22 models · 80 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.
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