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SeaSpine Spacer System - Hollywood VI NanoMetalene 34-8114-SRecalls & reported problems

Seaspine Orthopedics Corporation · Hollywood VI NM Sterile 11mm x 27mm x 14mm, Lordotic · Class 2 · Implant

Data updated Oct 18, 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 00889981034835), received between Jun 5, 2021 and Jun 5, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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 18, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • MalfunctionJun 5, 2021Fracture; Fracture

    A PATIENT UNDERWENT SPINAL SURGERY ON (B)(6) 2021 CONSISTING OF SEASPINE'S HOLLYWOOD NANOMETALENE INTERBODY SYSTEM. IT WAS REPORTED THAT THE INTERBODY FRACTURED DURING INSERTION AND THE CAGE TURNED AND BECAME STUCK IN THE DISC SPACE. THE SURGEON WAS ABLE TO RECOVER THE IMPLANT; HOWEVER, THE REPORTER WAS NOT ABLE TO CONFIRM THAT ALL FRAGMENTS WERE RETRIEVED.

    Patient problems: Failure of Implant

    MAUDE report 11943784 ↗

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Sources and updates

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