RABEA 5° Cervical cage, angledRecalls & 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
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 04047844000151), received between Oct 12, 2020 and Oct 12, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Inaccurate Information” (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
- Inaccurate Information1
- Labelling, Instructions for Use or Training Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 12, 2020Labelling, Instructions for Use or Training Problem; Inaccurate Information; Labelling, Instructions for Use or Training Problem; Inaccurate Information
A CUSTOMER COMPLAINT HAS REVEALED THAT THE FOLLOWING MEDICAL DEVICE: REF: WK041214; RABEA PEEK CERVICAL CAGE ANGLED 4X12X14MM 5°, LOT 818192-KT - CONTAINS ITEM PK041214, RABEA PEEK - CERVICAL CAGE PARALLEL 4X12X14MM 0°. OUR FIRST INVESTIGATIONS REVEALED THAT A WRONG LABELLING OCCURRED IN THE FRAMEWORK OF THE MANUFACTURING PROCESS. ONLY THE PRODUCT MENTIONED ABOVE AND ONLY THAT SINGLE LOT NUMBER IS AFFECTED. THE DEVICE IN QUESTION WAS NOT DELIVERED TO U.S. MARKET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10661105 ↗
Other Intervertebral Fusion Device With Bone Graft, Cervical devices
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- ROI-C MC1005TLDR Spine Usa, Inc. · Intervertebral Fusion Device With Bone Graft, Cervical54 reports
- EIT CIF cage CUI8060LEIT Emerging Implant Technologies GmbH · Intervertebral Fusion Device With Bone Graft, Cervical1 recall1 report
- CONSTRUX - MINI PTC 37-5012SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-6211SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-7308SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-9207SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI Ti 37-6106SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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