MotoBAND™ CP DynaForce® MPJ MPJ Short 5deg Valgus/0deg DorsiflexionRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00815432026364), received between Dec 24, 2020 and Jan 2, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).

1 other recall cover devices cleared under the same FDA submission (K173710); they may or may not involve this specific model.

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 18, 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.

• MalfunctionJan 2, 2024Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

  IT WAS REPORTED THAT DURING A PROCEDURE ON (B)(6) 2023, THE DRILL GUIDE TOWER WOULD NOT THREAD CORRECTLY ONTO THE PLATE IN QUESTION. THE SURGEON BELIEVED THERE WAS AN ISSUE WITH THE THREADS. SURGERY CONTINUED BY OPENING A NEW PLATE, THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO ADVERSE PATIENT IMPACT. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR A MTP PL, STD 18MM STAPLE, 0°, STERILE. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: Insufficient Information

  MAUDE report 18427394 ↗
• MalfunctionDec 24, 2020Fracture; Appropriate Device Problem Term/Code Not Available; Fracture; Appropriate Device Problem Term/Code Not Available

  AT ROUTINE FOLLOW-UP THE SURGEON NOTED THAT THE MPJ PLATE WAS BROKEN AT THE FUSION SITE APPROXIMATELY 3 MONTHS AFTER THE INITIAL SURGERY. THE PATIENT WAS NON-WEIGHT BEARING FOR 2 WEEKS THEN WEIGHT BEARING FOR 8 WEEKS. THE SURGEON GOT A CT SCAN AND DETERMINED FUSION WOULD NOT LIKELY OCCUR. THE SURGEON REMOVED THE DEVICE WITHOUT COMPLICATION AND PLACE NON-CROSSROADS DEVICES ON (B)(6) 2020.

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 11072281 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K173710. One submission often covers many models, so check the product and lot details in each record.

• Z-0212-2020 · Sep 19, 2019 · Terminated
  MotoBand CP, Poly-axial Locking Screw, 3.0mm x 28mm