Device adverse event reports (MAUDE)

MiniMed 780G US System BLE Connect 3.0 mg/dL · Alternate Controller Enabled Insulin Infusion Pump

Medtronic Puerto Rico Operations Co. · Power Problem

2026-08-31MalfunctionInitial submissionMDR 50204214

Manufacturer contact zip ext

-386

Manufacturer link flag

Manufacturer g1 city

Juncos

Manufacturer contact address 1

Ceiba Norte Ind. Park #50 Road

Event type

Malfunction

Report number

2032227-2026-220290

Product problem flag

Date received

20260831

PMA pmn number

P160017

Date of event

20260801

Reprocessed and reused flag

Manufacturer contact zip code

00777

Reporter occupation code

003

Noe summarized

Manufacturer contact l name

Patel

Manufacturer g1 postal code

00777-3869

Reporter country code

Date added

20260831

Manufacturer contact f name

Keya

Device date of manufacturer

20240405

Reporter state code

Suppl dates mfr received

08/18/2026

Mfr report type

Thirty-Day

Manufacturer contact country

Date changed

20260901

Health professional

Summary report flag

Manufacturer g1 zip code ext

-386

Date report

20260831

Initial report to FDA

Manufacturer g1 country

Manufacturer contact city

Juncos

MDR report key

50204214

Date manufacturer received

20260802

Report source code

Manufacturer report

Manufacturer g1 zip code

00777

Manufacturer g1 name

Medtronic Puerto Rico Operations Co.

Adverse event flag

Single use flag

Manufacturer g1 address 1

Ceiba Norte Ind. Park #50 Road

Manufacturer contact postal code

00777-3869

Suppl dates FDA received

08/31/2026

Type of report

Initial submission, Followup

Source type

Consumer

Device

Device sequence number
408444
Date received
20260831
Brand name
MiniMed 780G US System BLE Connect 3.0 mg/dL
Generic name
Alternate Controller Enabled Insulin Infusion Pump
Manufacturer d name
Medtronic Puerto Rico Operations Co.
Manufacturer d address 1
Ceiba Norte Ind. Park #50 Road
Manufacturer d city
Juncos
Manufacturer d zip code
00777
Manufacturer d zip code ext
-386
Manufacturer d country
PR
Manufacturer d postal code
00777-3869
Device operator
LAY USER/PATIENT
Model number
MMT-1884
Catalog number
MMT-1884
Lot number
NG3750830H
Device availability
Yes
Date returned to manufacturer
20260817
Device report product code
QFG
Device evaluated by manufacturer
Y
Combination product flag
N
Harmonized identifiers (openFDA)
Device name
Alternate Controller Enabled Insulin Infusion Pump
Medical specialty description
Clinical Chemistry
Regulation number
880.5730
Device class
2

Product problems

Power Problem

Patient

Patient sequence number
1
Date received
20260831
Patient age
62 YR
Patient sex
Male
Patient weight
165 LB
Patient problems
No Clinical Signs, Symptoms or Conditions

How to read this: Each report says someone told FDA an event happened while a product was used. A report does not show the product caused it, and counts rise and fall with how many people report. Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.