Skip to content

SPOTLIGHT 282950900Recalls & reported problems

Depuy Spine, LLC · SPOTLIGHT PL LIGHT CABLE · Class 2

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 10705034359007), received between Jan 24, 2020 and Jan 24, 2020 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 24, 2020Break; Break

    IT WAS REPORTED ON AN UNKNOWN DATE, DURING A MITEK SALES SCHOOL EVENT DURING A SHOULDER PROCEDURE THE LIGHT CABLE WAS BROKEN. PATIENT AND PROCEDURE OUTCOME ARE UNKNOWN. THIS IS REPORT 1 OF 1 (B)(4).

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9629422 ↗

Other Light, surgical, instrument devices

All Light, surgical, instrument devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.