Pro Lift Instruments 151-265Recalls & reported problems
Life Spine, Inc. · Class 2 · Implant
Data updated Oct 16, 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 00190837031084), received between Aug 20, 2020 and Apr 2, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- No Known Impact Or Consequence To Patient1
- 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 2, 2024Fracture; Fracture
IT WAS REPORTED THAT "DURING DISC PREPATION, THE 7MM ROTATE SHAVER BROKE OFF IN THE L5-S1 SPACE. THERE WAS A 1-HOUR DELAY FOR MICROSCOPE TO BE BROUGHT IN TO AID IN SEEING FRGAMENTS. THE SURGEON HAD TO WIDEN THE DISC SPACE TO ACCESS THE BROKEN PIECE."
Patient problems: Unspecified Musculoskeletal problem
MAUDE report 19024637 ↗InjuryAug 20, 2020Break
TIP OF SHAVER BROKEN DURING SURGERY AND DELAYED SURGERY 40 MIN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10430607 ↗
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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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