Device brand name · For treatment purposes
HumaPen Luxura Half-Dose Pen: medical device reports filed with FDA
190 reports name it, 2011–2026. Manufacturer given most often on reports: Eli Lilly And. Product code FMF.
- 190
- device reports naming the brand
- 0% of all MAUDE reports · about 12 a year
- 11
- reports, 12 months to August 2026
- 8 in the 12 months before
- 3.2%
- classified as malfunction
- 88.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 190 reports that name the brand "HumaPen Luxura Half-Dose Pen" (for treatment purposes), received between February 2011 and August 2026; the manufacturer given most often on reports is Eli Lilly And. Spellings of one product vary from report to report.
11 reports arrived in the 12 months to August 2026, up 38% from 8 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 injury (96.8%) and malfunction (3.2%); across all syringe, piston reports (product code FMF) death is recorded in 0.1% and malfunction in 88.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are mechanical jam (19.5%), failure to deliver (16.3%) and break (13.2%). The patient problems coded most often are hyperglycemia, hypoglycemia and elevated ketones/ diabetic ketoacidosis. 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 53,081 reports carrying product code FMF. 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 |
|---|---|---|---|
| Mechanical jam | 37 | 19.5% | 0.8% |
| Failure to deliverthe device did not deliver the dose or item | 31 | 16.3% | 3.6% |
| Breakthe device broke | 25 | 13.2% | 9.2% |
| Insufficient device problem information | 18 | 9.5% | 0.9% |
| Device operates differently than expectedthe device behaved unexpectedly | 13 | 6.8% | 1% |
| Inaccurate delivery | 13 | 6.8% | 0.9% |
| Insufficient flow or under infusion | 12 | 6.3% | 0.7% |
| Improper or incorrect procedure or method | 11 | 5.8% | 0.6% |
| Excess flow or over-infusion | 8 | 4.2% | 0.3% |
| Mechanical problema mechanical problem | 8 | 4.2% | 0.6% |
| Crackthe device cracked | 6 | 3.2% | 2.6% |
| Fracturea broken bone | 5 | 2.6% | 0.2% |
| Defective devicethe device was defective | 4 | 2.1% | 1.7% |
| Device fell | 3 | 1.6% | 0.1% |
| Difficult or delayed activation | 3 | 1.6% | 0.2% |
| Infusion or flow problema problem with flow or infusion | 3 | 1.6% | 0.5% |
| Output problem | 3 | 1.6% | 0% |
| Application program problem: medication error | 2 | 1.1% | 0% |
| Detachment of device or device componentpart of the device came off | 2 | 1.1% | 1.2% |
| Device difficult to setup or prepare | 2 | 1.1% | 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 |
|---|---|---|
| Hyperglycemiahigh blood sugar | 103 | 54.2% |
| Hypoglycemialow blood sugar | 47 | 24.7% |
| Elevated ketones/ diabetic ketoacidosis | 13 | 6.8% |
| Coma | 10 | 5.3% |
| Overdosea dose above the recommended amount | 6 | 3.2% |
| Underdoseless than the intended dose | 6 | 3.2% |
| Malaisegeneral feeling of being unwell | 4 | 2.1% |
| Anxietyanxiety | 3 | 1.6% |
| Dizzinesslight-headedness or unsteadiness | 3 | 1.6% |
| Missed dose | 3 | 1.6% |
| Abdominal distention | 2 | 1.1% |
| Abdominal painstomach or belly pain | 2 | 1.1% |
| Fainting | 2 | 1.1% |
| Falla fall | 2 | 1.1% |
| Loss of consciousnesspassing out | 2 | 1.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | HumaPen Luxura Half-Dose Pen | Product code FMF | All MAUDE reports |
|---|---|---|---|
| Reports | 190 | 53,081 | 26,136,888 |
| Share of that pool | — | 0.4% | 0% |
| Classified as death, per 1,000 reports | 0 | 1 | 9 |
| Classified as injury | 96.8% | 9.9% | 36.2% |
| Classified as malfunction | 3.2% | 88.5% | 62.3% |
| Filed by the manufacturer | 100% | 93.7% | 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 FMF
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Inpen Mmt-105nnblna Novo Nordisk Blue | 1,620 | 188 | 0.1% |
| Inpen Mmt-105elblna Eli Lily Blue | 1,292 | 168 | 0.1% |
| Inpen Mmt-105nnpkna Novo Nordisk Pink | 1,142 | 219 | 0.1% |
| Rsvr Mmt-326a 10pk Prdgm 1 8ml 13l | 1,103 | 0 | 0.4% |
| Kit MMT-105NNBLW1 NovoNordisk Blue OUS1 | 1,011 | 655 | 0% |
| BD Luer-Lok | 1,001 | 333 | 0% |
| Inpen Mmt-105nngyna Novo Nordisk Gray | 972 | 143 | 0% |
| Unspecified Bd Syringe | 926 | 0 | 0.1% |
| Bd Insulin Syringe With The Bd Ultra-Fine Needle | 869 | 0 | 0% |
| Bd Ultra-Fine Insulin Syringe | 849 | 0 | 0% |
| Inpen Mmt-105elpkna Eli Lily Pink | 805 | 123 | 0% |
| Inpen Mmt-105elgyna Eli Lily Gray | 736 | 88 | 0% |
| Bd Luer-Lok Tip Syringe | 624 | 0 | 0% |
| Bd Luer-Lok Syringe | 595 | 0 | 0% |
| Novopen 4 | 567 | 67 | 0.7% |
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 HumaPen Luxura Half-Dose Pen reports
How many FDA reports name HumaPen Luxura Half-Dose Pen?
190 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 11 in the latest 12 months.
What kinds of events are reported?
injury (96.8%) and malfunction (3.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
mechanical jam (19.5%), failure to deliver (16.3%), break (13.2%), insufficient device problem information (9.5%) and device operates differently than expected (6.8%). 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 HumaPen Luxura Half-Dose Pen 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.