Devices › Cement, bone, vertebroplasty
Device brand name · Cement bone vertebroplasty
Vertecem V+ Cement Kit: medical device reports filed with FDA
701 reports name it, 2013–2026. Manufacturer given most often on reports: Synthes. Product code NDN.
- 701
- device reports naming the brand
- 0% of all MAUDE reports · about 52 a year
- 98
- reports, 12 months to August 2026
- 129 in the 12 months before
- 91.7%
- classified as malfunction
- 74.9% across the product code
- 0.1%
- classified as death, as reported
- 1 reports · not verified by FDA
FDA's MAUDE database holds 701 reports that name the brand "Vertecem V+ Cement Kit" (cement bone vertebroplasty), received between February 2013 and August 2026; the manufacturer given most often on reports is Synthes. Spellings of one product vary from report to report.
98 reports arrived in the 12 months to August 2026, down 24% from 129 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (91.7%), injury (8.1%) and death (0.1%); across all cement, bone, vertebroplasty reports (product code NDN) death is recorded in 1.9% and malfunction in 74.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are improper chemical reaction (42.1%), fluid/blood leak (21.5%) and failure to eject (20.3%). The patient problems coded most often are pain, nerve damage and appropriate clinical signs, symptoms and conditions term/code not available. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 4,843 reports carrying product code NDN. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Improper chemical reaction | 295 | 42.1% | 8.2% |
| Fluid/blood leak | 151 | 21.5% | 6.3% |
| Failure to eject | 142 | 20.3% | 4.3% |
| Breakthe device broke | 54 | 7.7% | 5% |
| Device operates differently than expectedthe device behaved unexpectedly | 40 | 5.7% | 1.9% |
| Chemical problem | 39 | 5.6% | 4% |
| Packaging problem | 12 | 1.7% | 0.6% |
| Migration or expulsion of device | 8 | 1.1% | 11.3% |
| Migrationthe device moved from where it was placed | 6 | 0.9% | 2.2% |
| Leak/splashthe device leaked | 5 | 0.7% | 12.5% |
| Device difficult to setup or prepare | 4 | 0.6% | 0.3% |
| Improper or incorrect procedure or method | 4 | 0.6% | 0.5% |
| Mechanical jam | 4 | 0.6% | 0.2% |
| Device difficult to maintain | 3 | 0.4% | 0.1% |
| Insufficient device problem information | 3 | 0.4% | 2% |
| Filling problem | 2 | 0.3% | 0.3% |
| Material integrity problema problem with the device material | 2 | 0.3% | 4.5% |
| Bent | 1 | 0.1% | 0.1% |
| Burst container or vessel | 1 | 0.1% | 0.4% |
| Clumping in device or device ingredient | 1 | 0.1% | 0.1% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Painpain, site not specified | 7 | 1% |
| Nerve damage | 6 | 0.9% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 5 | 0.7% |
| Joint laxity | 4 | 0.6% |
| No patient involvement | 4 | 0.6% |
| Bone fracture(s) | 3 | 0.4% |
| Embolism/embolus | 3 | 0.4% |
| Hypersensitivity/allergic reaction | 3 | 0.4% |
| Blood loss | 2 | 0.3% |
| Cardiac arrestthe heart stopped | 2 | 0.3% |
| Discomfortdiscomfort | 2 | 0.3% |
| Dyspneashortness of breath | 2 | 0.3% |
| Foreign body in patientpart of a device left in the patient | 2 | 0.3% |
| Inflammationinflammation | 2 | 0.3% |
| Injurya physical injury | 2 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Vertecem V+ Cement Kit | Product code NDN | All MAUDE reports |
|---|---|---|---|
| Reports | 701 | 4,843 | 26,136,888 |
| Share of that pool | — | 14.5% | 0% |
| Classified as death, per 1,000 reports | 1 | 19 | 9 |
| Classified as injury | 8.1% | 22.4% | 36.2% |
| Classified as malfunction | 91.7% | 74.9% | 62.3% |
| Filed by the manufacturer | 100% | 98.1% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code NDN
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Kyphx Hv-R Bone Cement | 916 | 7 | 3.4% |
| KYPHON HV-R Bone Cement | 314 | 110 | 0.3% |
| Confidence Kit No Needles | 175 | 8 | 5.1% |
| Confidence Spinal Cmt Sys 11c | 170 | 14 | 1.8% |
| KYPHON Xpede Bone Cement | 168 | 38 | 3% |
| Synflate Balloon/Medium- Sterile | 173 | 66 | 0% |
| Unknown_InstrumentstIre_Product | 1,475 | 123 | 0% |
| Unknown Instruments Product | 400 | 23 | 0.8% |
| Simplex P-Japanese Twin Pack | 312 | 1 | 10.6% |
| Stryker | 559 | 5 | 1.3% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Vertecem V+ Cement Kit reports
How many FDA reports name Vertecem V+ Cement Kit?
701 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 98 in the latest 12 months.
What kinds of events are reported?
malfunction (91.7%), injury (8.1%) and death (0.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
improper chemical reaction (42.1%), fluid/blood leak (21.5%), failure to eject (20.3%), break (7.7%) and device operates differently than expected (5.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Vertecem V+ Cement Kit was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.