ANCHORAGE PLP14341Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07613252260554), received between Jul 18, 2018 and Mar 5, 2026 — classified as 7 injuries, 1 malfunction.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryMar 5, 2026Migration

  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 7 HAD DEVICE DISPLACEMENT.

  Patient problems: Insufficient Information

  MAUDE report 24517185 ↗
• 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 159 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24495956 ↗
• 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 141 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24495337 ↗
• 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 145 HAD GENERALIZED PAIN.

  Patient problems: Pain

  MAUDE report 24495332 ↗
• InjuryApr 9, 2025Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT THE MTP PLATE WAS BROKEN AFTER IMPLANTATION IN THE PATIENT. THE PRIMARY SURGERY IN QUESTION WAS THE ARTHRODESIS FOR HALLUX VALGUS AND RIGIDUS. THE SURGEON HAS PERFORMED THE REVISION OPERATION ON THE BROKEN PLATE.

  Patient problems: Failure of Implant; Insufficient Information

  MAUDE report 21806635 ↗
• InjuryJun 28, 2023Break; Fracture; Break; Fracture

  AS REPORTED: "ARTHRODESIS 1ST MTP LEFT FOOT IN 04/22 BY PLATE. PSEUDARTHRODESIS WITH BROKEN PLATE. PATIENT REQUIRES REVISION SURGERY."

  Patient problems: Failure of Implant

  MAUDE report 17217791 ↗
• MalfunctionNov 16, 2019Material Twisted/Bent; Loose or Intermittent Connection; Material Twisted/Bent

  IT WAS REPORTED THAT DURING A PROCEDURE WHEN THE SCREW WAS INSERTED INTO THE LOCKING PLATE, IT STRIPPED THE THREAD OF THE PLATE SO THAT THE PLATE WOULD NO LONGER LOCK. IT WAS FURTHER REPORTED THAT THE CORRECT GUIDE, SCREW AND DRILL BIT WERE USED. THE PLATE WAS DISCARDED AND A NEW ONE WAS USED TO SUCCESSFULLY COMPLETE THE PROCEDURE.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 9333093 ↗
• InjuryJul 18, 2018Pressure Problem

  THE CUSTOMER REPORTED THAT THE PATIENT PRESENTED WITH PAIN IN HER FOOT, WHICH SHE HAD FOR 6 MONTHS FOLLOWING INITIAL IMPLANTATION WITH AN ANCHORAGE PLATE. THE PATIENT ALSO REPORTED THAT PART OF THE TOE DID NOT FLEX. THE PATIENT HAD 2 OPINIONS POST OPERATIVELY WHEN SHE PRESENTED WITH THE PAIN PLUS X-RAYS AND SCANS WHICH SHOWED NO ISSUE WITH THE PLATE. DURING A 3RD CONSULTATION, A SPECTORAL SCAN SHOWED PRESSURE IN AREAS OVER 4 OF THE 5 SCREWS. THE PLATE WAS REVISED.

  Patient problems: Pain

  MAUDE report 7700736 ↗