Prestige LP Streamlined InstrumentsRecalls & reported problems across all models

We found 3 models of Prestige LP Streamlined Instruments by Medtronic Sofamor Danek, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jan 4, 2026 and Jan 4, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (1 report).

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Prestige LP Streamlined Instruments recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Mar 13, 2018Terminated

   The firm received complaints of drill bits breaking during use with the Prestige LP(TM) Cervical Disc System. Subsequent investigation demonstrated the interaction of the drill guide and the drill bit may lead to drill bit breakage.

   Z-1641-2018 · Root cause: Under Investigation by firm · names 3 of these models · Recall details · FDA record ↗

Most reported Prestige LP Streamlined Instruments problems

Prestige LP Streamlined Instruments models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Prestige LP Streamlined Instruments 6975205

  Prosthesis, intervertebral disc
  1 recall1 report
• Prestige LP Streamlined Instruments 6975206

  Prosthesis, intervertebral disc
  1 recall0 reports
• Prestige LP Streamlined Instruments 6975207

  Prosthesis, intervertebral disc
  1 recall0 reports

Recent Prestige LP Streamlined Instruments adverse event reports

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

• MalfunctionJan 4, 2026Material Twisted/Bent

  INFORMATION WAS RECEIVED FROM USER FACILITY VIA A MANUFACTURER REPRESENTATIVE REGARDING A DEVICE USED FOR SPINAL THERAPY. IT WAS REPORTED THAT, THE 5 MM GUIDE WAS SLIGHTLY BENT AND THE TRIAL GETS WEDGED ON. THERE WAS NO PATIENT INVOLVEMENT REPORTED. NO FURTHER COMPLICATIONS REPORTED REGARDING THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23953809 ↗

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