SPOTLIGHT 282918570Recalls & reported problems
Depuy Spine, LLC · SPOTLIGHT ACCESS SYSTEM ILLUMINATED ANATOMIC PORT 18 x 70mm · Class 2
All models of SPOTLIGHT (16)
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 10705034206622), received between Feb 12, 2021 and Feb 12, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionFeb 12, 2021Break; Break
IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING ROUTINE INCOMING INSPECTION OF A LOANER SET, IT WAS OBSERVED THAT THE PORT WAS BROKEN. THERE WAS NO KNOWN PATIENT OR HOSPITAL INVOLVEMENT. THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS FOR (1) SPOT 18X70 ANATOMIC PORT. THIS IS REPORT 1 OF 1 (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11322773 ↗
Other RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY devices
- AURORA® Surgiscope® ASX15/60Integra Lifesciences Corporation · Retractor, Self-Retaining, For Neurosurgery1 recall1 report
- SPOTLIGHT 282915560Depuy Spine, LLC · RETRACTOR, SELF-RETAINING, FOR NEUROSURGERY2 reports
- 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
- 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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