ANCHORAGE PLSL3028Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613252262305), received between Dec 1, 2020 and Dec 1, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (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.

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.

• MalfunctionDec 1, 2020Positioning Failure; Positioning Failure

  AS REPORTED: "2 OF THE LOCKING SCREWS 3MM FROM THE ANCHORAGE FOOT SET HAVE NOT LOCKED INTO THE PLATE AND THE HEAD OF ANOTHER SCREW HAS BROKEN OFF."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10931137 ↗
• MalfunctionDec 1, 2020Positioning Failure; Positioning Failure

  AS REPORTED: "2 OF THE LOCKING SCREWS 3MM FROM THE ANCHORAGE FOOT SET HAVE NOT LOCKED INTO THE PLATE AND THE HEAD OF ANOTHER SCREW HAS BROKEN OFF."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10931124 ↗