ANCHORAGE PLSL3010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613252262091), received between Oct 3, 2019 and Dec 2, 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 2, 2020Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT THE 3.0MM SCREW DID NOT LOCK INTO THE PLATE. ADDITIONALLY REPORTED: CASE WAS COMPLETED BY USING A NEW SCREW. THERE WAS PREDRILLING PERFORMED, THE BONE WAS SOFT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10931520 ↗
• MalfunctionOct 3, 2019Positioning Failure; Appropriate Device Problem Term/Code Not Available; Positioning Failure

  AS REPORTED: "LOCKING SCREW WENT THROUGH PLATE. A NEW SCREW WAS USED AND IT FIT PERFECTLY ACCORDING TO THE SURGEON." ALSO REPORTED: "THE PLATE WAS IMPLANTED AND SO IT WOULD NOT BE POSSIBLE [TO OBTAIN CATALOG & LOT #]. IT CERTAINLY WASN¿T AN ISSUE WITH THE PLATE GIVEN THAT THE NEXT SCREW FIT PERFECTLY ACCORDING TO THE SURGEON. THE SURGEON TOOK THE SCREW OUT AND REPLACED IT WITH ANOTHER AND SO A DELAY OF SAY 1 MINUTE OCCURRED." PROCEDURE WAS OTHERWISE COMPLETED SUCCESSFULLY WITH NO ADVERSE CONSEQUENCES REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9153543 ↗