ANCHORAGE PLP30172Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613252260837), received between Aug 29, 2018 and Mar 3, 2026 — classified as 3 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Activation, Positioning or Separation Problem” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• 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 36 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24496445 ↗
• 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 151 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24495806 ↗
• InjuryFeb 24, 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 133 HAD GENERALIZED PAIN AND POST-OPERATIVE WOUND INFECTION.

  Patient problems: Pain; Post Operative Wound Infection

  MAUDE report 24429324 ↗
• MalfunctionJan 14, 2019Positioning Failure

  IT WAS REPORTED THAT THE SURGEON MADE A LISFRANC OPERATION WITH THE ANCHORAGE FOOT PLATING SYSTEM. THE PLATE WAS ALREADY IMPLEMENTED IN THE PATIENT WITH THREE LOCKING SCREWS AND ONE CORTICAL SCREW. THE LAST LOCK SCREW "CORKED" THROUGH THE LOCKING HOLE SO THAT IT NO LONGER LOCKED ONTO THE PLATE. SURGEON DECIDED TO REMOVE THE PLATE AND ALL THE SCREWS AND REPLACE THEM WITH NEW ONES. THE NEW PLATE AND SCREWS WORKED FINE. SURGICAL DELAY APPROX. 10 MINUTES. PLATE AND SCREWS WERE REMOVED AND REPLACED WITH NEW ONES.

  Patient problems: No Code Available

  MAUDE report 8246270 ↗
• MalfunctionAug 29, 2018Activation, Positioning or Separation Problem

  IT WAS REPORTED THAT SURGEON WAS PERFORMING AN ORIF MID FOOT ARTHRODESIS PROCEDURE - RIGHT SIDE AND WAS ATTEMPTING TO IMPLANT A 3.5 ACHORAGE SCREW, AND THE SCREW WENT THROUGH THE HOLE IN THE PLATE AND PROCEEDED TO GO ALL THE WAY THROUGH THE PLATE OUT THE BACK SIDE. SURGEON REMOVED PLATE AND SCREW AND WENT BACK IN WITH A NEW PLATE AND SCREWS AND COMPLETED THE CASE SUCCESFULLY AND WITH NO DELAY OR ADVERSE CONSEQUENCE TO THE PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7827323 ↗