ANCHORAGE PLP14342Recalls & reported problems
Stryker GmbH · Plate MTP CP, right · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 07613252260608), received between May 2, 2017 and Mar 3, 2026 — classified as 7 injuries, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (5 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.
Reports received per month
Most reported problems
Device problems
- Fracture5
- Break4
- Adverse Event Without Identified Device or Use Problem1
- Difficult to Insert1
Patient problems
- No Code Available3
- No Information2
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
- Pain1
Recent adverse event reports
The 8 most recent of 8 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 (B)(6) 2016 ¿ (B)(6) 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 54 HAD GENERALIZED PAIN
Patient problems: Pain
MAUDE report 24497077 ↗MalfunctionFeb 24, 2020Difficult to Insert; Difficult to Insert
PLATE FAILED TO ACCEPT LOCKING SCREWS. PROLONGED THE CASE BY 5 MINUTES TO SWITCH TO DIFFERENT PLATE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9748401 ↗InjuryApr 30, 2019Break; Fracture; Fracture
THE FOLLOWING EVENT WAS REPORTED TO THE ANSM: " MTP ARTHRODESIS PLATE RIGHT FOOT WAS IMPLANTED ON (B)(6)2016 , WAS FOUND BROKEN IN THE PATIENT'S FOOT. PATIENT WAS REVISED TO NEW PLATE.
Patient problems: No Information
MAUDE report 8566377 ↗InjuryMar 27, 2019Break; Fracture; Fracture
InjuryMar 26, 2019Break; Fracture; Fracture
IT WAS REPORTED THAT THE PLATE BROKE BETWEEN WEEK 2 AND WEEK 6 AFTER THE IMPLANTATION. POSTOPERATIVELY, NO SCREW LOOSENING WAS DETECTED. THE PLATE HAD TO BE REMOVED AND A NEW ARTHRODESIS HAD TO BE DONE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8453745 ↗InjuryDec 17, 2018Break
THE PHARMACIST FROM THE HOSPITAL REPORTED THE FOLLOWING EVENT: "PLATE FOR ARTHRODESIS MTP RIGHT FOOT 'ASKED THE' (B)(6) 2016, FOUND BROKEN IN THE FOOT OF THE PATIENT. CONSEQUENCES OF THE INCIDENT: CHANGING THE PLATE (1 PLATE, 2 SCREWS 18 AND 2 SCREWS 16)."
Patient problems: No Code Available
MAUDE report 8171046 ↗InjuryApr 30, 2018Fracture; Fracture
IT WAS REPORTED THAT DOCTOR REMOVED A BROKEN MTPCP PLATE ALONG WITH 3 MM KNOW I¿M LOCKING SCREWS AND REPLACED WITH A NEW PLATE AND 3.5 NO LOCKING SCREWS. PATIENT REQUIRED A REVISION SURGERY.
Patient problems: No Code Available
MAUDE report 7472242 ↗InjuryMay 2, 2017Fracture; Fracture
ANCHORAGE MTP CP PLATE HAS BROKEN ROUGHLY 9 WEEKS POST OP REQUIRING REVISION SURGERY.
Patient problems: No Code Available
MAUDE report 6539072 ↗
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- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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