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Cambria NanoMetalene 39-2609-SRecalls & reported problems

Seaspine Orthopedics Corporation · Cambria NM Implant,15 x 13 x 9mm,Lordotic,Sterile · 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 00889981064948), received between Apr 10, 2019 and Apr 10, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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

  • Patient-Device Incompatibility1

Patient problems

  • Patient Problem/Medical Problem1

Recent adverse event reports

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

  • MalfunctionApr 10, 2019Patient-Device Incompatibility; Patient-Device Incompatibility

    INDEX SURGERY (B)(6) 2018; MULTI-LEVEL ACDF C4-C7. REVISION TO REMOVE IMPLANT PERFORMED (B)(6) 2019 DUE TO C4/C5 NON-UNION IMPLANT AND REMOVAL OF A (COMPETITOR) BROKEN ANTERIOR PLATE AND SCREW.

    Patient problems: Patient Problem/Medical Problem

    MAUDE report 8501607 ↗

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Sources and updates

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