DynaFORCE™ 7120-2020KTRecalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00815432023394), received between Dec 4, 2019 and Sep 29, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (2 reports).
1 other recall cover devices cleared under the same FDA submission (K142727, K181410); 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 16, 2026.
Most reported problems
Device problems
- Fracture2
Patient problems
- Failure of Implant1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2022Fracture; Fracture
DOCTOR IMPLANTED A 20 MM DYNAFORCE CLIP ACROSS AN ALLOGRAFT WEDGE IN ORDER TO PROMOTE FUSION. DURING A ROUTINE FOLLOW UP VISIT, DOCTOR DISCOVERED THAT THE IMPLANT HAD FRACTURED IN BOTH LEGS. HE ALSO STATED THE ALLOGRAFT SEEMED TO BE EXPERIENCING FUSION. HOWEVER, HE WAS NOT CONFIDENT IN THE EXTENT OF THE FUSION. HE PLANS TO MONITOR THE PATIENT AND SEE IF THE JOINT CONTINUES TO EXHIBIT FUSION. DOCTOR DOES NOT CURRENTLY HAVE ANY PLANS TO REVISE OR EXPLANT THE HARDWARE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15501491 ↗InjuryDec 4, 2019Fracture; Fracture
NINE (9) MONTHS POST-OP BROKEN CLIP AND PLATE WERE IDENTIFIED. REVISION SURGERY WAS SCHEDULED FOR HARDWARE REMOVAL. THE DOCTOR CONFIRMED FUSION VIA X-RAY AND WILL NOT PLACE ADDITIONAL HARDWARE AFTER REMOVAL.
Patient problems: Failure of Implant
MAUDE report 9410446 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K142727, K181410. One submission often covers many models, so check the product and lot details in each record.
- Z-1487-2017 · Feb 16, 2017 · TerminatedMotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
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.
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