DynaFORCE™ 7125-2222KTRecalls & reported problems
Crossroads Extremity Systems · DynaFORCE is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis · Class 2 · Implant
All models of DynaFORCE (8)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00815432023400), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (1 report).
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
Device problems
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2022Fracture; Fracture
DOCTOR REPORTS THAT ON (B)(6) 2018 HE PERFORMED A MIDFOOT AND SUBTALAR FUSION CASE. HE USED CROSSROADS STAPLES IN THE MIDFOOT TO FUSE THE MEDIAL AND INTERMEDIATE CUNEIFORMS TO A NAVICULAR GRAFT FROM THE ILIAC CREST THAT WAS HARVESTED IN THE SAME SURGERY. THIS PATIENT HAD MUELLER WEISS SYNDROME WHICH IS AN ADULT ONSET OSTEONECROSIS OF THE TARSAL NAVICULAR. AT SOME POINT POST-OPERATION ONE OF THE CLIP LEGS BROKE IN THE PATIENT. DOCTOR SAYS THE BONES EVENTUALLY FUSED EVEN THOUGH ONE OF THE CLIP LEGS WAS BROKEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501693 ↗
Other Staple, Fixation, Bone devices
- N/A StandardSynthes GmbH · Staple, Fixation, Bone2 recalls16 reports
- GII QUICKANCHOR ETHIBOND 212034Medos International Sàrl · STAPLE, FIXATION, BONE98 reports
- GII QUICKANCHOR ORTHOCORD 222983Medos International Sàrl · STAPLE, FIXATION, BONE94 reports
- Speed SE-0910Synthes GmbH · Staple, Fixation, Bone1 recall24 reports
- Speed Shift SE-2020-10Synthes GmbH · Staple, Fixation, Bone1 recall10 reports
- Lapiplasty SpeedPlate SK50Treace Medical Concepts, Inc. · Staple, Fixation, Bone59 reports
- Speed SE-1512Synthes GmbH · Staple, Fixation, Bone1 recall6 reports
- LUPINE ORTHOCORD 210709Depuy Mitek, LLC · STAPLE, FIXATION, BONE56 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page