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SPOTLIGHT 282924550Recalls & reported problems

Depuy Spine, LLC · SPOTLIGHT ACCESS SYSTEM ILLUMINATED ANATOMIC PORT 24 x 50mm · 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 10705034207421), received between Apr 29, 2020 and Apr 29, 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. 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 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.

  • MalfunctionApr 29, 2020Break; Break

    DEVICE REPORT FROM CANADA REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT THE SPOTLIGHT TUBE BROKE DURING A SPINAL FUSION SURGERY ON (B)(6) 2020. NO FRAGMENTS WERE RETAINED. A SIMILAR INSTRUMENT WAS USED FOR THE REMAINDER OF THE PROCEDURE. THERE WERE NO PATIENT CONSEQUENCES. THIS REPORT IS FOR A SPOT 24X50 ANATOMIC PORT. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10011445 ↗

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Sources and updates

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