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NUBIC Cervical cageRecalls & reported problems

SIGNUS Medizintechnik GmbH · The basic shape of the NUBIC and RABEA devices is a rectangular frame. The upper and lower aspects of the implant are open with surface spikes which assist in the positive anchorage and seating between the superior and inferior vertebral bodies. The device is available in a variety of sizes enabling the surgeon to choose the size best suited to the individual pathology and anantomical condition. A connecting screw is available which permits attachment of the NUBIC (without strut) to the SIGNUS TOSCA II anterior cervical plate if the surgeon so chooses. · Class 2 · Implant

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 04047844010563), received between Oct 15, 2019 and Oct 15, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (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

  • Manufacturing, Packaging or Shipping Problem1
  • No Apparent Adverse Event1
  • Nonstandard Device1
  • Product Quality Problem1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionOct 15, 2019Nonstandard Device; Product Quality Problem; Manufacturing, Packaging or Shipping Problem; No Apparent Adverse Event; Nonstandard Device; Product Quality Problem; Manufacturing, Packaging or Shipping Problem; No Apparent Adverse Event

    A CUSTOMER COMPLAINT HAS REVEALED THAT THE FOLLOWING PRODUCT REF: NB071317, NUBIC PEEK CERVICAL CAGE 7X13X17MM, LOT 816889-AV CONTAINS A WRONG PRODUCT. THIS WRONG PRODUCT IS NOT INTENDED FOR TREATMENT OF THE CERVICAL SPINAL COLUMN AND IS NOT COMPATIBLE WITH THE NUBIC SURGICAL INSTRUMENTS.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9189985 ↗

Other Intervertebral Fusion Device With Bone Graft, Cervical devices

All Intervertebral Fusion Device With Bone Graft, Cervical devices →

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