Devices › Alternate controller enabled insulin infusion pump
Device brand name · Omnipod 5 pods
Omnipod 5 Pods: medical device reports filed with FDA
53,253 reports name it, 2024–2026. Manufacturer given most often on reports: Insulet. Product code QFG.
- 53,253
- device reports naming the brand
- 0.2% of all MAUDE reports · about 22,856 a year
- 34,593
- reports, 12 months to August 2026
- 18,505 in the 12 months before
- 92.2%
- classified as malfunction
- 88.9% across the product code
- 0%
- classified as death, as reported
- 7 reports · not verified by FDA
53,253 medical device reports received by FDA name the brand "Omnipod 5 Pods" (omnipod 5 pods); the manufacturer given most often on reports is Insulet; received from March 2024 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
34,593 reports arrived in the 12 months to August 2026, up 87% from 18,505 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 (92.2%) and injury (7.7%); across all alternate controller enabled insulin infusion pump reports (product code QFG) death is recorded in 0% and malfunction in 88.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are unintended movement (46.3%), loss of or failure to bond (43.2%) and material twisted/bent (19.3%). The patient problems coded most often are hyperglycemia, erythema 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 1,297,995 reports carrying product code QFG. 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 |
|---|---|---|---|
| Unintended movement | 24,679 | 46.3% | 6.6% |
| Loss of or failure to bond | 22,987 | 43.2% | 6.1% |
| Material twisted/bent | 10,275 | 19.3% | 2.7% |
| Fluid/blood leak | 6,221 | 11.7% | 1.6% |
| Failure to fire | 5,453 | 10.2% | 1.3% |
| Insufficient device problem information | 4,950 | 9.3% | 3.2% |
| Difficult to insertthe device was hard to insert | 4,808 | 9% | 1.2% |
| Activation, positioning or separation problem | 2,508 | 4.7% | 0.6% |
| Premature activation | 2,411 | 4.5% | 0.5% |
| Communication or transmission problemthe device could not communicate or transmit | 678 | 1.3% | 4.7% |
| Retraction problem | 564 | 1.1% | 0.2% |
| Difficult or delayed activation | 515 | 1% | 0.1% |
| Material split, cut or torn | 511 | 1% | 0.1% |
| Obstruction of flow | 344 | 0.6% | 6.4% |
| Device alarm system | 84 | 0.2% | 0.1% |
| Leak/splashthe device leaked | 58 | 0.1% | 0.7% |
| Corrodedthe device corroded | 45 | 0.1% | 0% |
| Device dislodged or dislocated | 43 | 0.1% | 0% |
| Incorrect, inadequate or imprecise result or readings | 43 | 0.1% | 0% |
| Excess flow or over-infusion | 28 | 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 |
|---|---|---|
| Hyperglycemiahigh blood sugar | 41,951 | 78.8% |
| Erythemaskin redness | 1,677 | 3.1% |
| Elevated ketones/ diabetic ketoacidosis | 1,467 | 2.8% |
| Hemorrhage/blood loss/bleeding | 1,402 | 2.6% |
| Vomitingbeing sick | 1,309 | 2.5% |
| Painpain, site not specified | 1,065 | 2% |
| Swelling/ edema | 974 | 1.8% |
| Nauseafeeling sick | 830 | 1.6% |
| Skin inflammation/ irritation | 627 | 1.2% |
| Hypoglycemialow blood sugar | 513 | 1% |
| Fatiguetiredness | 409 | 0.8% |
| Dizzinesslight-headedness or unsteadiness | 395 | 0.7% |
| Headachehead pain | 371 | 0.7% |
| Skin infection | 365 | 0.7% |
| Loss of consciousnesspassing out | 282 | 0.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Omnipod 5 Pods | Product code QFG | All MAUDE reports |
|---|---|---|---|
| Reports | 53,253 | 1,297,995 | 26,136,888 |
| Share of that pool | — | 4.1% | 0.2% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 7.7% | 11.1% | 36.2% |
| Classified as malfunction | 92.2% | 88.9% | 62.3% |
| Filed by the manufacturer | 100% | 99.9% | 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 QFG
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| t:slim X2 Insulin Pump with Control-IQ Technology | 584,236 | 129,119 | 0% |
| t:slim X2 Insulin Pump with Interoperable Technology (with t:connect mobile app) | 267,716 | 11,502 | 0% |
| Omnipod 5 Pod | 72,516 | 13,913 | 0.1% |
| t:slim X2 Insulin Pump with Control-IQ+ Technology | 65,298 | 57,936 | 0% |
| iLet Bionic Pancreas | 62,887 | 60,771 | 0.1% |
| Omnipod 5 Automated Insulin Delivery System | 50,523 | 32,478 | 0% |
| t:slim X2 Insulin Pump with Interoperable Technology | 37,136 | 865 | 0% |
| Tandem Mobi Insulin Pump with Control-IQ+ Technology | 36,506 | 31,674 | 0% |
| Tandem Mobi Insulin Pump with Interoperable Technology | 27,952 | 1,595 | 0% |
| Tandem Mobi Insulin Pump with Control-IQ Technology | 15,154 | 9,553 | 0% |
| MiniMed 780G US System BLE Connect 3.0 mg/dL | 112,817 | 57,140 | 0.1% |
| t:slim X2 Insulin Pump with Basal-IQ Technology | 142,641 | 1,916 | 0% |
| Omnipod 5 Controller | 2,618 | 926 | 0.8% |
| T Slim X2 Insulin Pump With Interoperable Technology With T Connect Mobile A | 2,555 | 0 | 0% |
| PUMP MMT-1884L MM780G BLE 3.0 mg/ml | 34,846 | 9,703 | 0.1% |
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 Omnipod 5 Pods reports
How many FDA reports name Omnipod 5 Pods?
53,253 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 34,593 in the latest 12 months.
What kinds of events are reported?
malfunction (92.2%) and injury (7.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
unintended movement (46.3%), loss of or failure to bond (43.2%), material twisted/bent (19.3%), fluid/blood leak (11.7%) and failure to fire (10.2%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%) and voluntary reports (0%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Omnipod 5 Pods 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.