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 · TerminatedMedtronic 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 · TerminatedMedtronic 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 · TerminatedExtremities, 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 · TerminatedKyphon 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 · TerminatedKyphX Xpander Inflatable Bone Tamp, size 15/3, Catalog Number K09A, Manufactured by Kyphon Sarl, Switzerland. For use in spinal surgery.
Other ARTHROSCOPE devices
- FMS 283512Medos International Sàrl · ARTHROSCOPE1,800 reports
- Arthrex® AR-6480Arthrex, Inc. · ARTHROSCOPE949 reports
- FMS VUE 284002Depuy Mitek, LLC · ARTHROSCOPE829 reports
- MITEK 242018Medos International Sàrl · Arthroscope731 reports
- METRx® System 9560100Medtronic Sofamor Danek, Inc. · Arthroscope667 reports
- FMS VUE II 284004Medos International Sàrl · Arthroscope562 reports
- VAPR COOLPULSE 228146Depuy Mitek, LLC · ARTHROSCOPE474 reports
- FMS DUO 284580Depuy Mitek, LLC · ARTHROSCOPE458 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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