Devices › Pump, infusion, insulin
Device brand name · Insulin infusion pump / sensor augmented
Model Not Specified: medical device reports filed with FDA
773 reports name it, 2004–2023. Manufacturer given most often on reports: Medtronic Minimed. Product code LZG.
- 773
- device reports naming the brand
- 0% of all MAUDE reports · about 35 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 39.8%
- classified as malfunction
- 81.6% across the product code
- 5.3%
- classified as death, as reported
- 41 reports · not verified by FDA
FDA's MAUDE database holds 773 reports that name the brand "Model Not Specified" (insulin infusion pump / sensor augmented), received between August 2004 and August 2023; the manufacturer given most often on reports is Medtronic Minimed. Spellings of one product vary from report to report.
0 reports arrived in the 12 months to August 2026, and none 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 (54.7%), malfunction (39.8%) and death (5.3%); across all pump, infusion, insulin reports (product code LZG) death is recorded in 0.3% and malfunction in 81.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are insufficient device problem information (23%), device displays incorrect message (21.2%) and failure to deliver (6.2%). 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 539,975 reports carrying product code LZG. 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 |
|---|---|---|---|
| Insufficient device problem information | 178 | 23% | 5% |
| Device displays incorrect message | 164 | 21.2% | 6.8% |
| Failure to deliverthe device did not deliver the dose or item | 48 | 6.2% | 0.5% |
| Bent | 43 | 5.6% | 1.4% |
| Device operates differently than expectedthe device behaved unexpectedly | 40 | 5.2% | 4.7% |
| Improper or incorrect procedure or method | 26 | 3.4% | 1.1% |
| Air leak | 24 | 3.1% | 0.3% |
| Fluid/blood leak | 22 | 2.8% | 2.2% |
| Inaccurate delivery | 19 | 2.5% | 1.7% |
| Device alarm system | 13 | 1.7% | 1.2% |
| Device inoperablethe device could not be used | 13 | 1.7% | 2.6% |
| Improper flow or infusion | 12 | 1.6% | 0.1% |
| Leak/splashthe device leaked | 12 | 1.6% | 0.7% |
| No display/image | 11 | 1.4% | 3.1% |
| Breakthe device broke | 10 | 1.3% | 2.9% |
| Excess flow or over-infusion | 10 | 1.3% | 0.3% |
| High test results | 10 | 1.3% | 0.4% |
| Infusion or flow problema problem with flow or infusion | 5 | 0.6% | 0.2% |
| Kinkedthe tube or line kinked | 5 | 0.6% | 0.5% |
| Nonstandard device | 5 | 0.6% | 0.4% |
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 | 248 | 32.1% |
| Hypoglycemialow blood sugar | 111 | 14.4% |
| Elevated ketones/ diabetic ketoacidosis | 103 | 13.3% |
| Hospitalization required | 42 | 5.4% |
| Deaththe patient died; cause not stated by this term | 40 | 5.2% |
| Loss of consciousnesspassing out | 23 | 3% |
| Vomitingbeing sick | 20 | 2.6% |
| Blood glucose, high | 17 | 2.2% |
| Nauseafeeling sick | 17 | 2.2% |
| Coma | 13 | 1.7% |
| Injurya physical injury | 13 | 1.7% |
| Blood glucose, low | 12 | 1.6% |
| Overdosea dose above the recommended amount | 10 | 1.3% |
| Underdoseless than the intended dose | 9 | 1.2% |
| Dehydrationdehydration | 7 | 0.9% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Model Not Specified | Product code LZG | All MAUDE reports |
|---|---|---|---|
| Reports | 773 | 539,975 | 26,136,888 |
| Share of that pool | — | 0.1% | 0% |
| Classified as death, per 1,000 reports | 53 | 3 | 9 |
| Classified as injury | 54.7% | 17.8% | 36.2% |
| Classified as malfunction | 39.8% | 81.6% | 62.3% |
| Filed by the manufacturer | 100% | 99.8% | 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 LZG
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Onetouchping Glucosemgmtsystem | 98,945 | 0 | 0.1% |
| Omnipod DASH Insulin Management System | 62,646 | 5,563 | 0.1% |
| Tandem T Slim Insulin Delivery System | 55,207 | 0 | 0.1% |
| OmniPod Insulin Pump | 45,272 | 145 | 0.3% |
| Omnipod Insulin Management System | 37,582 | 218 | 0.1% |
| Animas Vibe | 88,703 | 0 | 0% |
| Animas Insulin Infusion Pump | 26,293 | 0 | 0.3% |
| MMT-712 PARADIGM Insulin Pump | 25,781 | 4,138 | 0% |
| Accu-Chek Spirit Combo | 21,252 | 0 | 0.1% |
| t:slim Insulin Delivery System | 19,277 | 30 | 0.1% |
| t:slim X2 Insulin Pump | 31,159 | 86 | 0% |
| Animas Insulin Cartridge | 12,105 | 0 | 0% |
| T Flex Insulin Delivery System | 11,359 | 0 | 0.1% |
| Paradigm Insulin Infusion Pump | 16,324 | 0 | 0.4% |
| Accu-Chek Spirit | 8,826 | 0 | 0.3% |
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 Model Not Specified reports
How many FDA reports name Model Not Specified?
773 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
injury (54.7%), malfunction (39.8%) and death (5.3%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
insufficient device problem information (23%), device displays incorrect message (21.2%), failure to deliver (6.2%), bent (5.6%) and device operates differently than expected (5.2%). 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 Model Not Specified 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.