CONTOUR®NEXT 7550Recalls & reported problems
Ascensia Diabetes Care US Inc. · Blood glucose test strips. Sold in a carton of 15 test strips. · Class 3
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10301937550154), received between Mar 10, 2020 and Mar 10, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “High Readings” (1 report).
23 other recalls cover devices cleared under the same FDA submission (K191286, K193407, K210687, K223293, K241787, P150001, P160017); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- High Readings1
Patient problems
- Confusion/ Disorientation1
- Loss of consciousness1
- Seizures1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 10, 2020High Readings; High Readings
AN ADVOCATE REPORTED THAT THE CUSTOMER OBTAINED A BLOOD GLUCOSE READING OF 336 MG/DL AT 12:19 P.M. ON THE CONTOUR NEXT LINK 2.4 METER. BASED ON THIS READING, THE CUSTOMER TOOK AN UNKNOWN AMOUNT OF INSULIN BOLUS FROM THE INSULIN PUMP. UPON REPEAT TESTING, THE CUSTOMER OBTAINED THE FOLLOWING READINGS: 156 MG/DL AT 2:18 P.M., 79 MG/DL AT 5:26 P.M. AND 58 MG/DL AT 10:18 P.M. WITH THE READING OF 79 MG/DL, THE CUSTOMER EXPERIENCED SYMPTOMS OF HYPOGLYCEMIA SUCH AS CONFUSION AND LOSS OF CONSCIOUSNESS. THE CUSTOMER WENT TO THE HOSPITAL WHERE HE HAD A SEIZURE. NO TREATMENT DETAILS FOR THE HYPOGLYCEMIC EVENT WAS PROVIDED. THE CUSTOMER WAS DISCHARGED FROM THE HOSPITAL ON (B)(6) 2020. THE ADVOCATE WAS ADVISED TO RETURN THE DEVICE FOR EVALUATION. REPLACEMENT METER AND TEST STRIPS WERE SENT TO THE CUSTOMER.
Patient problems: Confusion/ Disorientation; Loss of consciousness; Seizures
MAUDE report 9810453 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K191286, K193407, K210687, K223293, K241787, P150001, P160017. One submission often covers many models, so check the product and lot details in each record.
- Z-2981-2026 · Jul 13, 2026 · Open, ClassifiedMiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
- Z-1740-2026 · Feb 13, 2026 · Open, ClassifiedMiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
- Z-1739-2026 · Feb 13, 2026 · Open, ClassifiedMiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
- Z-1742-2026 · Feb 13, 2026 · Open, ClassifiedMiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
- Z-1265-2025 · Jan 31, 2025 · Open, ClassifiedMiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
- Z-1261-2025 · Jan 31, 2025 · Open, ClassifiedMiniMed insulin pump, REF: 670G (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
- Z-1259-2025 · Jan 31, 2025 · Open, ClassifiedMiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
- Z-1266-2025 · Jan 31, 2025 · Open, ClassifiedMiniMed insulin pump, REF: 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)
- Z-0001-2025 · Jul 31, 2024 · Open, ClassifiedMiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF: MMT-1800, MMT-1801, MMT-1805, MMT-1850, MMT-1851
- Z-0003-2025 · Jul 31, 2024 · Open, ClassifiedMiniMed Insulin Pump Device. MiniMed 670G, REF: MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762; MiniMed 770G
- Z-2211-2023 · May 19, 2023 · Open, ClassifiedContour next GEN Blood Glucose Monitoring System
- Z-0193-2023 · Sep 20, 2022 · Open, ClassifiedInsulin Pump/Model: MiniMed 630G/ MMT-1715, MMT-1755, MMT-1754; MiniMed 670G/ MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1740, MMT-1741, MMT-1742
- Z-0855-2022 · Jan 27, 2022 · Open, ClassifiedMiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; MiniMed 770G: MMT-1880, MMT-18
- Z-1771-2021 · Mar 15, 2021 · Open, ClassifiedMiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL; PUMP MMT-1886 MM780G 6.5W BLE MG; KIT MMT-1895WW MM780G 6.5V BLE SF MMOL; KIT MMT-1896WW MM780G 6.5W BLE
- Z-0516-2021 · Apr 30, 2020 · Open, ClassifiedMiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under
…and 8 more.
Other Automated Insulin Dosing Device System, Single Hormonal Control devices
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls78 deaths55,723 reports
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control2 recalls51 deaths33,713 reports
- MiniMed®670G MMT-1780KPKMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls39 deaths28,789 reports
- MiniMed® 670G MMT-1780KLMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls8 deaths8,353 reports
- MiniMed® 670G MMT-1780KMedtronic Minimed, Inc. · Artificial pancreas device system, single hormonal control3 recalls7 deaths6,776 reports
- MiniMed® 670G MMT-1780KPKMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control3 recalls10 deaths4,325 reports
- MiniMed™ Reservoir MMT-332AMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control2 deaths3,013 reports
- Guardian™ Sensor (3) MMT-7020AMedtronic Minimed, Inc. · Automated insulin dosing device system, single hormonal control1,304 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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