Foot Plates MTPR-7Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842188120015), received between Mar 9, 2023 and Mar 4, 2026 — classified as 1 injury, 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 4, 2026Break

  SALES REP REPORTED ON (B)(6) 2026 THAT DURING A ROUTINE POST-OP APPOINTMENT, A SURGEON FOUND A BROKEN MTPR-7 THROUGH X-RAYS. IT WAS REPORTED THAT THE PATIENT IS NOT EXPERIENCING ANY PAIN SO THE SURGEON HAS OPTED TO LEAVE THE DEVICE INSITU AND PLANS TO SEE THE PATIENT BACK IN 6 MONTHS. AS OF (B)(6) 2026 IT IS UNKNOWN IF LEAVING THE DEVICE IMPLANTED WILL CAUSE THE PATIENT ANY ADDITIONAL HARM, THERE IS NO PATIENT INFORMATION AND THERE IS NO KNOWLEDGE IF THE PATIENT HAS FOLLOWED ALL POST-OP INSTRUCTIONS. AS OF (B)(6) 2026 THE DEVICE REMAINS IMPLANTED.

  Patient problems: Failure of Implant

  MAUDE report 24509772 ↗
• InjuryMar 9, 2023Break; Break

  (B)(6) REPORTED ON (B)(6) 2023 THAT A SURGEON REMOVED A MTPR-7 PLATE FROM A PATIENT DUE TO A BREAK AT THE JOINT LINE BECAUSE THE MPJ DID NOT FUSE. ALL HARDWARE WAS SUCCESSFULLY REMOVED FROM THE PATIENT AND AN ARTHROPLASTY REVISION WAS PERFORMED AFTER REMOVAL. THE REMOVAL SURGERY DID NOT HAVE ANY DELAYS. THE HARDWARE IS AVAILABLE FOR RETURN BUT NO PICTURES OR X-RAYS HAVE BEEN PROVIDED.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 16518527 ↗