ANCHORAGE PLP10341Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07613252260417), received between Apr 26, 2019 and Mar 3, 2026 — classified as 6 injuries.

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

• 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 162 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24496103 ↗
• 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 8 HAD REVISION.

  Patient problems: Insufficient Information

  MAUDE report 24495802 ↗
• 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 3 HAD GENERALIZED PAIN AND NONUNION.

  Patient problems: Malunion of Bone; Pain

  MAUDE report 24429320 ↗
• 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 105 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24429119 ↗
• InjuryMay 15, 2023Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT ABOUT 7 MONTHS AFTER A LEFT TOE FUSION, THE PATIENT DEVELOPED SUDDEN PAIN WITH WALKING AND RETURNED TO THEIR DOCTOR FOR EVALUATION. X-RAYS WERE TAKEN AND SHOW FRACTURES IN THE PLATE. THE DEVICE WAS REMOVED FROM THE PATIENT.

  Patient problems: Failure of Implant; Implant Pain

  MAUDE report 16929681 ↗
• InjuryApr 26, 2019Break; Fracture; Fracture

  PLATE BROKE APPROX. 10 WEEKS AFTER IMPLANTATION. PATIENT WAS REVISED.

  Patient problems: No Code Available

  MAUDE report 8554776 ↗