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KyphoPak™ Express™ Tray KPE1001-CDSRecalls & reported problems

Medtronic Sofamor Danek, Inc. · CEMENTSYS KPE1001-CDS FF EXPRESS 10/2 · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169456006), received between Sep 3, 2019 and Sep 3, 2019 — classified as 1 injury.

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

5 other recalls cover devices cleared under the same FDA submission (K041454); 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

  • Chemical Problem1

Patient problems

  • Extravasation1
  • Pulmonary Embolism1

Recent adverse event reports

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

  • InjurySep 3, 2019Chemical Problem; Chemical Problem

    IT WAS REPORTED THAT THE PATIENT UNDERWENT UNKNOWN SPINAL SURGERY AT T7 DUE TO HEMANGIOMA. INTRA-OP, CEMENT EXTRAVASATION OCCURRED AFTER FILLING THE SATISFACTORY CEMENT DUE TO THIS PULMONARY EMBOLISM OCCURRED.

    Patient problems: Extravasation; Pulmonary Embolism

    MAUDE report 8954887 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K041454. One submission often covers many models, so check the product and lot details in each record.

  • Z-2390-2020 · Apr 24, 2020 · Terminated
    Medtronic Bone Void Filler, Small - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Kit c
  • Z-2391-2020 · Apr 24, 2020 · Terminated
    Medtronic Bone Void Filler, Large - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Kit c
  • Z-2389-2020 · Apr 24, 2020 · Terminated
    Extremities, Large Kit Assy, US, 15/3 - Product Usage: is an injectable, moldable and biocompatible calcium phosphate bone void filler. The single-use Medtronic Bone Void Filler Ki
  • Z-3175-2011 · Mar 23, 2011 · Terminated
    Kyphon brand KyphoPak Express Tray First Fracture, 15/2 with KyphX Osteo Introducer System; Catalog Number: KPE1003; Product is manufactured and distributed by Medtronic Spine LLC
  • Z-1209-2009 · Feb 4, 2009 · Terminated
    KyphX Xpander Inflatable Bone Tamp, size 15/3, Catalog Number K09A, Manufactured by Kyphon Sarl, Switzerland. For use in spinal surgery.

Other ARTHROSCOPE devices

All ARTHROSCOPE devices →

Sources and updates

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