ProLift Expandable Spacer System Post Pack 58-1228-0710DRecalls & reported problems
Life Spine, Inc. · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00190837021580), received between Dec 6, 2022 and Dec 6, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Device Slipped” (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.
Most reported problems
Device problems
- Device Slipped1
Patient problems
- Unspecified Musculoskeletal problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 6, 2022Device Slipped; Device Slipped
IT WAS REPORTED THAT THE CAGE MIGRATED POSTERIORLY INTO THE CANAL AND HAD TO BE UNEXPANDED, THEN REMOVED. THE SCREWS WERE LOOSE AND TO BE REPLACED 8.5MM SCREWS.
Patient problems: Unspecified Musculoskeletal problem
MAUDE report 15928977 ↗
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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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