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IDENTITI NanoTec 126-PRO-08141207-SRecalls & reported problems

Alphatec Spine, Inc. · IDENTITi NanoTec CERVICAL POROUS Ti SPACER, 8 x 14 x 12 mm, 7° · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190376416267), received between Jun 15, 2023 and Jun 15, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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

  • Device Dislodged or Dislocated1

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.

  • InjuryJun 15, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

    ON (B)(6) 2023, A PATIENT UNDERWENT A 2-LEVEL ANTERIOR CERVICAL DISCECTOMY AND FUSION PROCEDURE. AT THE 6-WEEK POSTOPERATIVE VISIT, A RADIOGRAPH REVEALED A SCREW BACKOUT AT THE INFERIOR LEVEL, ALONG WITH SUBSIDENCE OF THE CAGE AT C6-C7. REVISION SURGERY IS PLANNED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17135961 ↗

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Sources and updates

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