ProLift L151-690Recalls & reported problems
Life Spine, Inc. · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00190837154011), received between Sep 11, 2024 and Sep 22, 2026 — classified as 2 injuries, 6 malfunctions.
The most frequently reported specific device problem is “Fracture” (6 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture6
- Break1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
InjurySep 22, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854757 ↗InjurySep 15, 2026Fracture
MalfunctionMay 19, 2026Fracture
IT WAS STATED THAT, "PROLIFT INSERTER BROKE OFF DURING REMOVAL OF CAGE.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25221443 ↗MalfunctionApr 27, 2026Fracture
IT WAS STATED "PROLIFT INSERTER INNER CORE BROKE WHILE INSERTING CAGE INTO PATIENT, WE HAD TO FIND A WAY TO WIGGLE OUT THE CAGE INSERTER WHILE IT WAS INSERTED IN THE PATIENT AS IT NO LONGER HAD A HANDLE ON IT AND NEED TO POP OFF FROM THE CAGE. "
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25004522 ↗MalfunctionOct 15, 2025Fracture; Fracture
IT WAS STATED THAT, "DISTAL TIP OF PROLIFT INSERTER BROKE OFF AT L4-L5. 2 INSERTERS BROKE; COLLAPSED DISC SPACE, SHAVED TO AN 8 ONLY."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23290856 ↗MalfunctionAug 26, 2025Material Integrity Problem; Material Integrity Problem
IT WAS STATED, "IT BROKE UP SURGEON USING A MALLET AND TRYING TO INSERTER CAGE INTO A COLLAPSE DISC SPACE. BROKEN PIECE WAS RECOVERED.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22900044 ↗MalfunctionAug 8, 2025Fracture; Fracture
IT WAS STATED THAT, "TIP OF INSERTER BROKE DURING INSERTION."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22749453 ↗MalfunctionSep 11, 2024Break; Break
IT WAS STATED THAT "PROLIFT INSERTER BROKE INTO TWO PARTS. THE BREAK HAPPENED IN BETWEEN THE HANDLE AND THE SHAFT UPON THE INSERTION OF THE CAGE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20193392 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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