ANCHORAGE PLP11342Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613252260516), received between Feb 20, 2019 and Mar 3, 2026 — classified as 3 injuries, 3 malfunctions.

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

• InjuryMar 3, 2026Structural Problem

  THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 138 HAD STRUCTURAL PROBLEM.

  Patient problems: Insufficient Information

  MAUDE report 24497649 ↗
• InjuryMar 3, 2026Adverse Event Without Identified Device or Use Problem

  THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 146 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24495333 ↗
• InjuryMar 3, 2026Adverse Event Without Identified Device or Use Problem

  THE MANUFACTURER RECEIVED RWE REPORT NAMED "SAFETY AND PERFORMANCE OF THE ANCHORAGE AND ANCHORAGE 2 CP IMPLANTS UTILIZING THE PREMIER HEALTHCARE DATABASE" THAT CONTAINS COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF ANCHORAGE AND ANCHORAGE 2 CP. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN 1 JAN 2016 ¿ 30 MAR 2025 DURING THE REVIEW OF THE REPORT, IT WAS NOT POSSIBLE TO ESTABLISH A SPECIFIC DEVICE DETAIL, PATIENT INFORMATION, AND CURRENTLY NO ADDITIONAL DEVICE INFORMATION IS AVAILABLE; HOWEVER, PATIENT 149 HAD NONUNION.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 24495054 ↗
• MalfunctionJan 26, 2021Material Fragmentation; Device Damaged by Another Device; Material Fragmentation; Device Damaged by Another Device

  AS REPORTED: "PRIMARY PROCEDURE, RIGHT FIRST MTP. IT WAS REPORTED THAT WHEN THE DRILL GUIDE WAS SEATED INTO A HOLE OF THE PLATE AND AFTER DRILLING WAS DONE, A THREAD-LIKE PIECE OF METAL WAS SEEN IN THE PATIENT. THE PIECE WAS REMOVED BY THE SURGEON. SURGEON REPORTED THAT IT FELT AS THOUGH THE DRILL GUIDE DID NOT SEEM TO BE SEATING AS DEEPLY IN THE HOLE AS IT HAD IN THE PREVIOUS HOLES, AND BELIEVES THAT THE THREAD OF METAL WAS SHAVED OFF OF THE PLATE WHILE DRILLING. PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO DELAY."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11229114 ↗
• 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 11060307 ↗
• MalfunctionFeb 20, 2019Fitting Problem; Material Protrusion/Extrusion

  THE FOLLOWING EVENT WAS REPORTED BY CLINIC: DESPITE THE USE OF THE BARREL ON THE PLATE ANCHORAGE MTP RIGHT (REF PLP11342), THE SCREW DIAMETER 3 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 8356235 ↗