ProLift Micro 58-0832-0813MRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00190837141684), received between Jan 16, 2023 and Oct 16, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Device Tipped Over” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryOct 16, 2023Device Tipped Over; Device Tipped Over

  IT WAS REPORTED THAT: " [WE] WERE NOTIFIED BY THE SURGEON AND DISTRIBUTOR THAT THE PROLIFT MICRO FLIPPED OVER. THEY THINK IT WAS DUE TO THE SET SCREW FROM ANOTHER PEDICLE SCREW SYSTEM THAT UNATTACHED. THEREFORE, CREATING AN UNSTABLE CONSTRUCT. REVISION SURGERY TO BE SCHEDULED THE WEEK OF SEPT 18TH".

  Patient problems: Unspecified Musculoskeletal problem

  MAUDE report 17942066 ↗
• InjuryJan 16, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING RETRACTION BEFORE IMPLANT INSERTION, THE SURGEON MAY HAVE RETRACTED THE NERVES TOO MUCH. THE PATIENT SUFFERED DROP FOOT, PERMANENT NERVE DAMAGE. IT WAS ALSO REPOTED THAT THE SURGEON STATED THE DAMAGE WAS A RESULT OF OUR IMPLANT NOT BEING A TRUE 8MM IMPLANT.

  Patient problems: Nerve Damage

  MAUDE report 16174321 ↗