DynaFORCE Staple Instruments MOTOCLIP INSERTER ASSEMBLY, 10X10Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810112597820), received between Oct 25, 2024 and Apr 22, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K142727); 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.

• MalfunctionApr 22, 2025Break; Entrapment of Device; Break; Entrapment of Device

  IT WAS REPORTED THAT A PART OF THE MOTOCLIP STAPLE INSERTER BROKE WHILE DEPLOYING THE STAPLE DURING THE CASE; A FRAGMENT WAS GENERATED. THE SURGEON WAS ABLE TO FINISH THE CASE SUCCESSFULLY WITH NO SURGICAL DELAY; IT IS UNKNOWN IF THERE WERE PATIENT CONSEQUENCES.

  Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

  MAUDE report 21883537 ↗
• MalfunctionOct 25, 2024Break; Device Damaged Prior to Use; No Apparent Adverse Event; Break; Device Damaged Prior to Use; No Apparent Adverse Event

  IT WAS REPORTED THAT ON SEPTEMBER 30, 2024, THE SALES REPRESENTATIVE WAS SHIPPED A COMPLETE SET AS TRUNK STOCK. A MOTOCLIP INSERTER 10X10 INSTRUMENT IN THE SET WAS SENT BROKEN AND CANNOT BE USED. BROKEN METAL INSERTER TAB, TWO METAL PRONGS AT END OF THE INSERTER, INSTRUMENT CAME WITH ONE METAL TAB BROKEN OFF INTO A PIECE. THERE IS NO FACILITY, PROCEDURE, OR PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20537060 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142727. One submission often covers many models, so check the product and lot details in each record.

• Z-1487-2017 · Feb 16, 2017 · Terminated
  MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.