YUKON OCT Spinal SystemRecalls & reported problems across all models
VB Spine LLC · 54 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one YUKON OCT Spinal System model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 238
- Deaths reported
- 0
- Injuries reported
- 99
- Recalls
- 3
We found 54 models of YUKON OCT Spinal System by VB Spine LLC in the FDA's device registry (GUDID). Together they are named in 238 adverse event reports in the FDA's MAUDE database, received between Jul 17, 2019 and Apr 23, 2026 — classified as 99 injuries, 139 malfunctions.
The most frequently reported specific device problem is “Fracture” (125 reports).
3 FDA recall records name at least one of these models by its device identifier, 1 still open.
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
YUKON OCT Spinal 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.
- Jun 13, 2022Class IIOpen, Classified
Some of the rods in this lot were observed to have discoloration, later confirmed to be indication of trace amounts of inorganic phosphorous compound. This may produce a mild irritating or inflammatory response; adverse local tissue reactions may occur related to cytotoxicity with the nonconforming rod and surrounding tissue.
Z-1307-2022 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
- Dec 14, 2020Class IITerminated
The Yukon polyaxial screw used in the Yukon Spinal System was incorrectly laser marked with size 5.0 mm (diameter) & 24 mm (length).
Z-0931-2021 · Root cause: Employee error · Recall details · FDA record ↗
- Nov 3, 2020Class IITerminated
Shafts do not pass through the inner cannula of the Anti-Torque Alignment Tube from Lot KTGG due to a manufacturing nonconformance. This could result in a delay of surgery or result in surgical intervention later on.
Z-0520-2021 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Most reported YUKON OCT Spinal System problems
Device problems
- Fracture125
- Migration69
- Insufficient Device Problem Information14
- Mechanical Jam13
- Device Dislodged or Dislocated8
- Nonstandard Device8
- Break6
- Migration or Expulsion of Device6
Patient problems
- No Clinical Signs, Symptoms or Conditions145
- No Consequences Or Impact To Patient34
- Injury24
- Insufficient Information24
- Pain18
- Neck Pain8
- No Code Available5
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available4
YUKON OCT Spinal System models
54 models, most reported first. Each model has its own page with its reports, recalls and device details.
- YUKON OCT Spinal System 7601-10001APPLIANCE, FIXATION, SPINAL INTERLAMINAL60 reports
- YUKON OCT Spinal System 7601-90001Orthopedic manual surgical instrument1 recall7 reports
- YUKON OCT Spinal System 7601-04026APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 recall2 reports
- YUKON OCT Spinal System 7601-540120APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 recall0 reports
- YUKON OCT Spinal System 7601-05030Orthosis, cervical pedicle screw spinal fixation15 reports
- YUKON OCT Spinal System 7601-90003Orthopedic manual surgical instrument13 reports
- YUKON OCT Spinal System 7601-05026Orthosis, cervical pedicle screw spinal fixation11 reports
- YUKON OCT Spinal System 7601-05028APPLIANCE, FIXATION, SPINAL INTERLAMINAL11 reports
- YUKON OCT Spinal System 7601-04528APPLIANCE, FIXATION, SPINAL INTERLAMINAL10 reports
- YUKON OCT Spinal System 7601-04526APPLIANCE, FIXATION, SPINAL INTERLAMINAL8 reports
- YUKON OCT Spinal System 7601-05024APPLIANCE, FIXATION, SPINAL INTERLAMINAL8 reports
- YUKON OCT Spinal System 7601-05030M-G1Orthosis, cervical pedicle screw spinal fixation7 reports
- YUKON OCT Spinal System 7601-03514APPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- YUKON OCT Spinal System 7601-04530APPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- YUKON OCT Spinal System 7601-05032APPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- YUKON OCT Spinal System 7601-05034Orthosis, cervical pedicle screw spinal fixation5 reports
- YUKON OCT Spinal System 7601-05030MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL5 reports
- YUKON OCT Spinal System 7601-03526APPLIANCE, FIXATION, SPINAL INTERLAMINAL4 reports
- YUKON OCT Spinal System 7601-04012-G1Orthosis, cervical pedicle screw spinal fixation4 reports
- YUKON OCT Spinal System 7601-03512APPLIANCE, FIXATION, SPINAL INTERLAMINAL3 reports
- YUKON OCT Spinal System 7601-03516Orthosis, cervical pedicle screw spinal fixation3 reports
- YUKON OCT Spinal System 7601-03520Orthosis, cervical pedicle screw spinal fixation3 reports
- YUKON OCT Spinal System 7601-04030Orthosis, cervical pedicle screw spinal fixation3 reports
- YUKON OCT Spinal System 7601-04540Orthosis, cervical pedicle screw spinal fixation3 reports
- YUKON OCT Spinal System 7601-03524APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- YUKON OCT Spinal System 7601-04018APPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- YUKON OCT Spinal System 7601-04020MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- YUKON OCT Spinal System 7601-04024MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL2 reports
- YUKON OCT Spinal System 7601-04540MOrthosis, cervical pedicle screw spinal fixation2 reports
- YUKON OCT Spinal System 7601-05024MOrthosis, cervical pedicle screw spinal fixation2 reports
- YUKON OCT Spinal System 7601-42432Orthosis, cervical pedicle screw spinal fixation2 reports
- YUKON OCT Spinal System 7601-90138Orthopedic manual surgical instrument2 reports
- YUKON OCT Spinal System 7601-03510APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-03518Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-03522APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-03528Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-03530Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-03532Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-04020APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-04024APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-04034APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-03514MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-03522MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-03524MOrthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-04524MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-04530MOrthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-05028MAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-43042Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-03524-G1Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-04028-G1APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-05026-G1APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-04534M-G1Orthosis, cervical pedicle screw spinal fixation1 report
- YUKON OCT Spinal System 7601-05028M-G1APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- YUKON OCT Spinal System 7601-10001-G1APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
Recent YUKON OCT Spinal System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE NECK OF A YUKON POLYAXIAL SCREW 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 24973325 ↗MalfunctionFeb 26, 2026Fracture
A COMPANY REPRESENTATIVE REPORTED THAT THE NECK OF A YUKON POLYAXIAL SCREW FRACTURED POST-OPERATIVELY. REVISION SURGERY HAS NOT BEEN PERFORMED NOR SCHEDULED AT THIS TIME.
Patient problems: Insufficient Information
MAUDE report 24455577 ↗MalfunctionFeb 26, 2026Fracture
MalfunctionJan 22, 2026Migration
A COMPANY REPRESENTATIVE REPORTED THAT A YUKON SET SCREW MIGRATED APPROXIMATELY THREE WEEKS POST-OPERATIVELY. AT THIS TIME, REVISION SURGERY HAS NOT TAKEN PLACE NOR BEEN SCHEDULED.
Patient problems: Insufficient Information
MAUDE report 24150574 ↗MalfunctionDec 23, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT A YUKON POLYAXIAL SCREW FRACTURED POST-OPERATIVELY AND THAT IT IS UNKNOWN IF A REVISION SURGERY WILL BE PERFORMED.
Patient problems: Insufficient Information
MAUDE report 23882348 ↗InjuryDec 23, 2025Fracture; Fracture
IT WAS REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY SEVEN MONTHS POST-OPERATIVELY TO ADDRESS TWO FRACTURED YUKON POLYAXIAL SCREWS. IT WAS FURTHER REPORTED THAT THE FRACTURES WERE OBSERVED ON A 6-MONTH POST-OPERATIVE X-RAY. A PORTION OF THE SCREWS WERE EXPLANTED, HOWEVER THE FRACTURED SCREW SHANKS REMAINED IN THE PATIENT AND LOWER LEVELS WERE THEN FUSED. THIS REPORT CAPTURES THE SECOND OF TWO SCREWS.
Patient problems: Back pain; Insufficient Information
MAUDE report 23877176 ↗InjuryDec 23, 2025Fracture; Fracture
IT WAS REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY SEVEN MONTHS POST-OPERATIVELY TO ADDRESS TWO FRACTURED YUKON POLYAXIAL SCREWS. IT WAS FURTHER REPORTED THAT THE FRACTURES WERE OBSERVED ON A 6-MONTH POST-OPERATIVE X-RAY. A PORTION OF THE SCREWS WERE EXPLANTED, HOWEVER THE FRACTURED SCREW SHANKS REMAINED IN THE PATIENT AND LOWER LEVELS WERE THEN FUSED. THIS REPORT CAPTURES THE FIRST OF TWO SCREWS.
Patient problems: Back pain; Insufficient Information
MAUDE report 23877175 ↗MalfunctionDec 18, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT TWO YUKON POLYAXIAL SCREWS FRACTURED POST-OPERATIVELY AND THAT A REVISION SURGERY WILL BE PERFORMED. THIS REPORT CAPTURES THE FIRST OF TWO SCREWS.
Patient problems: Insufficient Information
MAUDE report 23843437 ↗MalfunctionDec 18, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT TWO YUKON POLYAXIAL SCREWS FRACTURED POST-OPERATIVELY AND THAT IT IS UNKNOWN IF A REVISION SURGERY WILL BE PERFORMED. THE DEVICES REMAIN IMPLANTED. THIS REPORT CAPTURES THE SECOND OF TWO SCREWS.
Patient problems: Insufficient Information
MAUDE report 23843248 ↗InjuryDec 9, 2025Migration; Migration
NO NEW INFORMATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Pain
MAUDE report 23764423 ↗InjuryDec 9, 2025Migration; Migration
NO NEW INFORMATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Pain
MAUDE report 23764421 ↗MalfunctionDec 8, 2025Fracture; Fracture
NO NEW INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23752509 ↗InjuryNov 14, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT A PATIENT UNDERWENT REVISION SURGERY TO ADDRESS TWO FRACTURED YUKON POLYAXIAL SCREWS. THIS REPORT CAPTURES THE FIRST OF TWO SCREWS.
Patient problems: Insufficient Information
MAUDE report 23562904 ↗InjuryNov 14, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT A PATIENT UNDERWENT REVISION SURGERY TO ADDRESS TWO FRACTURED YUKON POLYAXIAL SCREWS. THIS REPORT CAPTURES THE SECOND OF TWO SCREWS.
Patient problems: Insufficient Information
MAUDE report 23562861 ↗MalfunctionNov 6, 2025Fracture; Fracture
A COMPANY REPRESENTATIVE REPORTED THAT TWO YUKON POLYAXIAL SCREWS FRACTURED POST-OPERATIVELY. REVISION SURGERY HAS NOT TAKEN PLACE NOR BEEN SCHEDULED AND NO ADVERSE CONSEQUENCES WERE REPORTED. THIS REPORT CAPTURES THE FIRST OF TWO SCREWS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23493162 ↗
Other VB Spine LLC products
- EVEREST Spinal System77 models · 336 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
- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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