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Clydesdale™ Spinal System 2926250Recalls & reported problems

Medtronic Sofamor Danek, Inc. · CAGE 2926250 CLYDESDALE 22 6 DEG 12X50 · Class 2 · Implant

All models of Clydesdale Spinal System (25)

Data updated Oct 18, 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 00613994972477), received between Mar 10, 2020 and Mar 10, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

8 other recalls cover devices cleared under the same FDA submission (K113528, P000058); 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

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 10, 2020Break; Break

    IT WAS REPORTED THAT THE PATIENT PRESENTED WITH LUMBALGIA AT L3-L4 AND L4-L5; AND UNDERWENT OBLIQUE LUMBAR INTERBODY FUSION AT L2-L3 AND L3-L4. INTRA-OP, THE CAGE BROKE. NO FRAGMENT OF THE BROKEN CAGE REMAINED INSIDE THE PATIENT. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9811904 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K113528, P000058. One submission often covers many models, so check the product and lot details in each record.

  • Z-0440-2019 · Sep 27, 2018 · Terminated
    INFUSE Bone Graft X SMALL KIT REF 7510100
  • Z-1593-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, SMALL KIT, REF 7510200AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1589-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, SMALL KIT, REF 7510200, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1591-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, LARGE KIT, REF 7510600, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1594-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1592-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft,LARGE II KIT, REF 7510800, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1590-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, MEDIUM KIT, REF 7510400, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic
  • Z-1595-2013 · May 28, 2013 · Terminated
    INFUSE(R) Bone Graft, LARGE II KIT, REF 7510800AUS, Medtronic Sofamore Danek USA, Inc., 1800 Pyramid Place, Memphis, Tennessee 38132 orthopaedic

Other Intervertebral fusion device with bone graft, lumbar devices

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page