SPOTLIGHT 282915560Recalls & reported problems
Depuy Spine, LLC · SPOTLIGHT ACCESS SYSTEM ILLUMINATED ANATOMIC PORT 15 x 60mm · Class 2
All models of SPOTLIGHT (16)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034206189), received between Nov 14, 2023 and Apr 5, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Slipped” (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.
Reports received per month
Most reported problems
Device problems
- Device Slipped1
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 5, 2024Mechanical Problem; Mechanical Problem
DEVICE REPORT FROM THE UNITED ARAB EMIRATES REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2023, THE SPOTLIGHT SYSTEM PORT FAILED DURING LAMINECTOMY SURGERY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO ADVERSE PATIENT IMPACT. NO FURTHER INFORMATION IS AVAILABLE TO REPORT. THIS REPORT IS FOR A SPOTLIGHT ACCESS SYSTEM ILLUMINATED ANATOMIC PORT 15 X 60MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19052437 ↗MalfunctionNov 14, 2023Device Slipped; Device Slipped
DEVICE REPORT FROM DEPUY SYNTHES REPORTS AN EVENT IN CHINA AS FOLLOWS: IT WAS REPORTED THAT DURING THE PROCEDURE ON OCTOBER 21, 2023, IT WAS NOTED THAT THE FRONT END OF THE DEVICE CHANNEL WAS LOOSE AND ROTATABLE. IT WAS CHANGED TO ANOTHER ONE TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT HARM OR SURGICAL DELAY. THIS REPORT IS FOR ONE (1) SPOT 15X60 ANATOMIC PORT THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18135928 ↗
Other RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY devices
- AURORA® Surgiscope® ASX15/60Integra Lifesciences Corporation · Retractor, Self-Retaining, For Neurosurgery1 recall1 report
- V. Mueller T-1295Steris Corporation · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- AURORA® Surgiscope® ASX15/80Integra Lifesciences Corporation · Retractor, Self-Retaining, For Neurosurgery1 report
- Aurora® Surgiscope® ASX9/100Integra Lifesciences Corporation · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- SPOTLIGHT 282918570Depuy Spine, LLC · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
- Symmetry KARLIN™ 46-3191Aspen Surgical Products, Inc. · Retractor, Self-Retaining, For Neurosurgery1 report
- Symmetry KARLIN™ 46-3204Aspen Surgical Products, Inc. · Retractor, Self-Retaining, For Neurosurgery1 report
- SPOTLIGHT 282924550Depuy Spine, LLC · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY1 report
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 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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