MotoCLIP™ 1442-1814Recalls & reported problems
Crossroads Extremity Systems · MotoCLIP™ is a bone staple for use in surgery of the hand and foot bone fragment osteotomy fixation and joint arthrodesis · Implant
Data updated Oct 18, 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 00850310006106), received between Jan 10, 2017 and Dec 3, 2019 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
Device problems
- Break1
- Fracture1
Patient problems
- Failure of Implant1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 3, 2019Fracture; Fracture
THE DOCTOR PERFORMED A SURGERY ON (B)(6) 2017 AND USED A 18X14MM MOTOCLIP IMPLANT. SIX (6) MONTHS POST OP THE PATIENT REQUESTED THAT THE IMPLANT BE REMOVED AND A REVISION SURGERY WAS PERFORMED. DURING THE REVISION SURGERY, THE DOCTOR NOTICED THE IMPLANT WAS LOOSE AND REMOVED ONLY THE BRIDGE. THE CLIP LEGS REMAIN IN THE PATIENT. THE DOCTOR CONFIRMED FUSION BY XRAY AT THE SURGICAL SITE. THE CLIP DID NOT APPEAR BROKEN ON THE XRAY. NO ADDITIONAL HARDWARE WAS IMPLANTED DURING THE REVISION SURGERY.
Patient problems: Failure of Implant
MAUDE report 9406431 ↗MalfunctionJan 10, 2017Break
PATIENT REQUESTED REMOVAL OF HARDWARE AFTER SUCCESSFUL FUSION. JOINT WAS PROPERLY FUSED AND PATIENT IS NON-SYMPTOMATIC. ELECTIVE SURGERY TO REMOVE HARDWARE. AT TIME OF REMOVAL ONE LEG OF THE STAPLE BROKE DURING THE REMOVAL PROCESS AND WAS LEFT IN THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6239640 ↗
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 · TerminatedMotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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