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TRANSCEND NanoTec 110-PRO-07161407-SRecalls & reported problems

Alphatec Spine, Inc. · TRANSCEND NanoTec CERVICAL PEEK SPACER, 7 x 16 x 14 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190376420899), received between Jun 23, 2023 and Jun 23, 2023 — classified as 1 malfunction.

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
  • Device Slipped1

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.

  • MalfunctionJun 23, 2023Device Slipped; Device Dislodged or Dislocated; Device Slipped; Device Dislodged or Dislocated

    A PATIENT UNDERWENT A 3-LEVEL ANTERIOR CERVICAL DISCECTOMY AND FUSION PROCEDURE ON (B)(6) 2022. AROUND 6-MONTHS POSTOPERATIVELY, RADIOGRAPH IMAGES REVEALED A SCREW BACK OUT AT THE SUPERIOR LEVEL, ALONG WITH SUBSIDENCE OF THE CAGES. THERE ARE NO PLANS FOR REVISION SURGERY. THE SURGEON WILL CONTINUE TO MONITOR THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17191299 ↗

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Sources and updates

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