ANCHORAGE PLP11341Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613252260493), received between Mar 4, 2020 and Mar 5, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Fracture” (3 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryMar 5, 2026Fracture

  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 (B)(6) HAD DEVICE BREAKAGE.

  Patient problems: Insufficient Information

  MAUDE report 24517023 ↗
• 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 136 HAD STRUCTURAL PROBLEM.

  Patient problems: Insufficient Information

  MAUDE report 24497489 ↗
• InjuryJun 17, 2025Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT: "MTP ANCHORAGE 1 PLATE BROKE WITHIN 2 WEEKS OF BEING IMPLANTED. THERE'S "PERSISTENT PAIN FROM PATIENT, CONFIRMED BY XRAY. XRAY CONFIRMED 2 WEEKS POST OP THAT THE PLATE HAD BROKE, REVISION SURGERY 2.5 MONTHS FROM PRIMARY SURGERY."

  Patient problems: Pain

  MAUDE report 22242348 ↗
• InjuryMar 4, 2020Fracture; Fracture

  THE PHARMACIST AT THE HOSPITAL REPORTED THE FOLLOWING EVENT : "ON (B)(6) 2019, THE PATIENT HAD AN ARTHRODESIS AT THE BIG TOE PERFORMED AS FOLLOWS: 1 FIXOS 4.0 SCREW + ONE 5-HOLE ANCHORAGE PLATE, 5 VALGUS SCREWS: 10°- DORSAL FLEXION: 20 °. ON (B)(6) 2020, THE PATIENT PRESENTED A PREMATURE RUPTURE OF HIS PLATE, PROBABLY IN CONNECTION WITH MECHANICAL STRESSES AND UNDERWENT A REVISION SURGERY TO REMOVE THE DEVICES WITH ADDITIONAL BONE GRAFTING AND IMPLANTATION OF A LARGER PLATE AND MORE COMPRESSION SCREWS."

  Patient problems: Failure of Implant; Injury

  MAUDE report 9789449 ↗