ProLift 58-1028-1210KRecalls & reported problems
Life Spine, Inc. · Class 2 · Implant
All models of ProLift (8)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190837086527), received between Jun 23, 2022 and Apr 1, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Expulsion” (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.
Reports received per month
Most reported problems
Device problems
- Expulsion1
- Mechanical Jam1
Patient problems
- Fall1
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Musculoskeletal problem1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 1, 2026Mechanical Jam
IT WAS STATED THAT " THE FIRST IMPLANT WE USED WE HAD TO WASTES DUE TO IT NOT EXPANDING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24753966 ↗InjuryJun 23, 2022Expulsion; Expulsion
IT WAS REPORTED THAT THE PATIENT FELL FROM A STANDING POSITION APPROXIMATELY A MONTH OUT FROM SURGERY. L5 INFERIOR SCREWS BROKE OUT OF THE PEDICLE INFERIORITY AND THE PROLIFT CAGE RETROPULSED POSTERIORLY, LATERAL TO THE SPINAL CANAL.
Patient problems: Fall; Unspecified Musculoskeletal problem
MAUDE report 14788271 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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