ANCHORAGE PLP10461Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613252260424), received between Jun 25, 2018 and Feb 24, 2026 — classified as 3 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. 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.

• 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 95 HAD GENERALIZED PAIN

  Patient problems: Pain

  MAUDE report 24428922 ↗
• InjuryMar 2, 2023Break; Fracture; Break; Fracture

  AS REPORTED: "FRACTURE OF MTP PLATE FROM ANCHORAGE SYSTEM WHICH RESULTED IN A REVISION SURGERY".

  Patient problems: Failure of Implant

  MAUDE report 16467592 ↗
• MalfunctionMar 26, 2019Material Fragmentation

  THE HOSPITAL PHARMACY REPORTED TO THE SALES REP AN EVENT REGARDING AN ARTHRODESIS PLATE REF: (B)(4). IN WHICH THEY INDICATE PRESENCE OF METAL FRAGMENTS OBSERVED AFTER DRILLING AND INSERTING OF THE SCREWS INTO THE PLATE. FEEDBACK RECEIVED FROM THE SURGEON ON MARCH 6TH INDICATE THAT HE DOES NOT CONFIRM THE ADVERSE EVENT. HE INDICATED THAT HE GAVE TOO MUCH ANGULATION TO HIS SCREW, WHICH DURING THE SCREWING PROCESS DEPOSITED A TITANIUM THREAD WHICH WAS REMOVED. HE WAS NOT EVEN INFORMED OF THE DECLARATION OF MATERIAL VIGILANCE BY THE PHARMACY. THE SURGEON HAS COMPLETED HIS OPERATION AND IS VERY SATISFIED WITH IT. NO CLINICAL CONSEQUENCES, NO DELAY IN INTERVENTION AND NO ADDITIONAL INTERVENTION.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8453743 ↗
• InjuryJun 25, 2018Break

  IT IS ALLEGED BY THE ATTORNEY THROUGH THE FILING OF A LEGAL CLAIM, THAT THE PATIENT UNDERWENT SURGERY FOR A LAPIDUS BUNIONECTOMY ON (B)(6) 2017 WHERE SHE WAS IMPLANTED WITH A LEFT STRYKER MTP ANCHORAGE PLATE IN HER RIGHT FOOT. IT IS FURTHER ALLEGED THAT ON (B)(6) 2018, WHILE WALKING IN HER CAM BOOT, SHE FELT AND HEARD A CRACK IN HER FOOT AND BEGAN TO EXPERIENCE PAIN AND SWELLING. X-RAYS REVEALED THE PLATE STABILIZING HER FIRST METATARSAL HAD BROKEN, WHICH REQUIRED REVISION SURGERY ON (B)(6) 2018. THEY FURTHER ALLEGE THE PLATE WAS BROKEN THROUGH AT THE POINT OF ONE OF THE SCREW HOLES.

  Patient problems: Failure of Implant; Pain; Swelling

  MAUDE report 7635367 ↗