ZEVO™ Anterior Cervical Plate System 7724015Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00643169329102), received between Dec 13, 2022 and Dec 13, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Migration” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K141632); they may or may not involve this specific model.

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 13, 2022Migration; Migration

  INFORMATION WAS RECEIVED FROM HEALTHCARE PROVIDER (HCP) VIA A MANUFACTURER REPRESENTATIVE REGARDING A PATIENT HAVING SPINAL THERAPY FOR UNKNOWN INDICATION. IT WAS REPORTED THAT AFTER SURGERY, THE SCREW WAS SEVERELY DETACHED AND COULD NOT BE RE-FIXED, WHICH EVENTUALLY LED TO RE-SURGERY AND PRODUCT REPLACEMENT. PRODUCTS EXPLANTED. THERE WERE NO PATIENT SYMPTOMS OR COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. ADDITIONAL INFORMATION RECEIVED FROM MANUFACTURER REPRESENTATIVE THAT THE SCREW MIGRATED FROM INTENDED LOCATION WAS THE ACTUAL ALLEGATION. THERE WERE NO ALLEGATION OR ADVERSE EVENT ASSOCIATED WITH THE PALATE. REVISION SURGERY WAS PERFORMED ONE MONTH AFTER SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15967528 ↗
• InjuryDec 13, 2022Migration; Migration

  INFORMATION WAS RECEIVED FROM HEALTHCARE PROVIDER (HCP) VIA A MANUFACTURER REPRESENTATIVE REGARDING A PATIENT HAVING SPINAL THERAPY FOR UNKNOWN INDICATION. IT WAS REPORTED THAT AFTER SURGERY, THE SCREW WAS SEVERELY DETACHED AND COULD NOT BE RE-FIXED, WHICH EVENTUALLY LED TO RE-SURGERY AND PRODUCT REPLACEMENT. PRODUCTS EXPLANTED. THERE WERE NO PATIENT SYMPTOMS OR COMPLICATIONS REPORTED AS A RESULT OF THIS EVENT. ADDITIONAL INFORMATION RECEIVED FROM MANUFACTURER REPRESENTATIVE THAT THE SCREW MIGRATED FROM INTENDED LOCATION WAS THE ACTUAL ALLEGATION. THERE WERE NO ALLEGATION OR ADVERSE EVENT ASSOCIATED WITH THE PALATE. REVISION SURGERY WAS PERFORMED ONE MONTH AFTER SURGERY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15967522 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K141632. One submission often covers many models, so check the product and lot details in each record.

• Z-1750-2018 · Mar 23, 2018 · Terminated
  Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW, REF 7710015, Size 4.5mm x 15mm Product Appliance, fixation, spinal intervertebral body