ProLift Lateral L151-695Recalls & reported problems
Life Spine, Inc. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00190837142254), received between Jan 3, 2023 and Jan 28, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJan 28, 2026Fracture
TIPS FROM SHORT10/12MM INSERTER BROKE INSITU. SURGEON WAS ABLE TO RETRIEVE THE BROKEN TIPS USING THE SUCTION, SO NOTHING WAS RETAINED IN THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24201591 ↗MalfunctionAug 18, 2025Fracture; Fracture
IT WAS STATED THAT "TIP OF INSERTER BROKE OFF."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22833149 ↗MalfunctionJan 3, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE INSERTER WAS STUCK TO THE IMPLANT WHEN TRYING TO REMOVE AFTER INSERTION. THERE WAS A 10 MINUTE SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16087902 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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