Foot Plates MTPL-7Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842188120022), received between May 23, 2025 and Feb 5, 2026 — classified as 2 injuries.

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 5, 2026Break

  SALES REP REPORTED ON (B)(6) 2026 THAT A SURGEON REPORTED A BROKEN MTPL-7 FOUND AFTER PERFORMING POST OP X-RAYS (DATE OF X-RAYS ARE UNKNOWN) BUT THE ORIGINAL IMPLANT DATE WAS (B)(6) 2025. THE SURGEON PLANS TO REMOVE THE HARDWARE/ CULTURE AND SEE HOW THE PATIENT DOES HOWEVER THE REVISION CASE IS NOT SCHEDULED. AFTER 6 FOLLOW-UP ATTEMPTS TO COLLECT INFORMATION ABOUT THE PATIENT, POTENTIAL CAUSES AND INFORMATION FROM THE SURGEON, THE REP STATED HE DOES NOT HAVE A LOT OF INFORMATION TO PROVIDE BUT HE KNOWS THE JOINT DID NOT HEAL. AS OF (B)(6) 2026 TRIMED HAS NOT RECEIVED ANY ADDITIONAL INFORMATION REGARDING THE STATUS OF WHEN THE REMOVAL SURGERY WILL TAKE PLACE. X-RAYS WERE PROVIDED BUT AS OF (B)(6) 2026 THE DEVICE REMAINS IMPLANTED.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 24273708 ↗
• InjuryMay 23, 2025Break; Fracture; Break; Fracture

  A SALES REP REPORTED ON 02MAY2025 THAT UPON X-RAY REVIEW DURING A POST-OP APPOINTMENT, THE SURGEON DISCOVERED A NON-UNION AFTER THE MTPL-7 WAS IMPLANTED ON (B)(6) 2024. IT IS UNKNOWN IF THE PATIENT FOLLOWED ALL POST-OP INSTRUCTIONS AND THIS WAS THE FIRST POST OP APPOINTMENT WHERE THE ISSUE WAS IDENTIFIED. A REVISION SURGERY IS SCHEDULED FOR (B)(6) 2025. ADDITIONAL INFORMATION WAS PROVIDED ON 08MAY2025 THAT THE HARDWARE WAS REMOVED SUCCESSFULLY. THE SURGEON SAID THE PATIENT CAN BE PAIN FREE AFTER A REMOVAL LIKE THIS SO CHOSE NOT TO PUT ANY ADDITIONAL HARDWARE IN AT THIS TIME EVEN THOUGH THE JOINT DID NOT FUSE. X-RAYS WERE PROVIDED AND IT IS UNKNOWN IF THE DEVICE WILL BE AVAILABLE TO BE RETURNED.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 22079964 ↗