ANCHORAGE PLSL3014Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613252262138), received between May 22, 2018 and Dec 22, 2020 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Device Operates Differently Than Expected” (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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 22, 2020Positioning Failure; Positioning Failure

  "IT WAS REPORTED THAT: "THE SCREWS COULD NOT BE SCREWED ON THE PLATE DELAY OF INTERVENTION NO PATIENT CONSEQUENCES"

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11060387 ↗
• MalfunctionFeb 20, 2019Fitting Problem

  THE FOLLOWING EVENT WAS REPORTED BY CLINIC: " DESPITE THE USE OF THE BARREL ON THE PLATE ANCHORAGE MTP RIGHT (REF PLP11342), THE SCREW DIAMETER3 LOCKING DOES NOT FIT CORRECTLY IN THE HOLE. THREADING PROBLEM WAS OBSERVED AND 1 WIRE CAME OUT OF THE SCREW. THE SCREW PROTRUDES FROM THE PLATE AND A METAL WIRE COMES OUT OF THE SCREW. THE SCREW WAS REMOVED AND ANOTHER SCREW REINSERTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8356287 ↗
• MalfunctionMay 22, 2018Device Operates Differently Than Expected

  AS REPORTED: WHILE IMPLANTING THE ANCHORAGE PLATE, THE DOCTOR SCREWED THE 3.0MM LOCKING SCREWS THROUGH THE MTP V1 PLATE [THREE] TIMES WITH ONLY "TWO FINGERS" WORTH OF FORCE. THIS WAS 3 SEPARATE SCREWS, EACH IN A SEPARATE HOLE. NONE OF THE SCREWS WERE EXPLANTED. THE DOCTOR JUST BACKED THEM UP FLUSH WITH THE PLATE AND LEFT THEM IN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7531486 ↗
• MalfunctionMay 22, 2018Device Operates Differently Than Expected

  AS REPORTED: WHILE IMPLANTING THE ANCHORAGE PLATE, THE DOCTOR SCREWED THE 3.0MM LOCKING SCREWS THROUGH THE MTP V1 PLATE [THREE] TIMES WITH ONLY "TWO FINGERS" WORTH OF FORCE. THIS WAS 3 SEPARATE SCREWS, EACH IN A SEPARATE HOLE. NONE OF THE SCREWS WERE EXPLANTED. THE DOCTOR JUST BACKED THEM UP FLUSH WITH THE PLATE AND LEFT THEM IN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7531482 ↗
• MalfunctionMay 22, 2018Insufficient Device Problem Information

  AS REPORTED: WHILE IMPLANTING THE ANCHORAGE PLATE, THE DOCTOR SCREWED THE 3.0MM LOCKING SCREWS THROUGH THE MTP V1 PLATE [THREE] TIMES WITH ONLY "TWO FINGERS" WORTH OF FORCE. THIS WAS 3 SEPARATE SCREWS, EACH IN A SEPARATE HOLE. NONE OF THE SCREWS WERE EXPLANTED. THE DOCTOR JUST BACKED THEM UP FLUSH WITH THE PLATE AND LEFT THEM IN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7531480 ↗
• MalfunctionMay 22, 2018Insufficient Device Problem Information

  AS REPORTED: WHILE IMPLANTING THE ANCHORAGE PLATE, THE DOCTOR SCREWED THE 3.0MM LOCKING SCREWS THROUGH THE MTP V1 PLATE [THREE] TIMES WITH ONLY "TWO FINGERS" WORTH OF FORCE. THIS WAS 3 SEPARATE SCREWS, EACH IN A SEPARATE HOLE. NONE OF THE SCREWS WERE EXPLANTED. THE DOCTOR JUST BACKED THEM UP FLUSH WITH THE PLATE AND LEFT THEM IN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7531477 ↗