Accu-Chek Guide Link 08109257001Recalls & reported problems
Roche Diagnostics Operations, Inc. · ACCU-CHEK GUIDE LINK MG/DL 118 (US) · Class 3
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00365702702134), received between Jun 30, 2021 and Apr 15, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Fire” (2 reports).
14 other recalls cover devices cleared under the same FDA submission (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fire2
- Display Difficult to Read1
- Melted1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 15, 2024Display Difficult to Read; Display Difficult to Read
IT WAS REPORTED THAT THE DISPLAY OF THE BLOOD GLUCOSE MONITOR APPEARED TO BE BURNT. THE CALLER REPORTED THAT THERE IS A BLACK SPOT WITH A WHITE RING AROUND IT, IN THE MIDDLE OF THE DISPLAY, THAT APPEARS TO BE A BURN MARK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19106949 ↗MalfunctionNov 16, 2023Fire; Fire
THE CALLER REPORTED THAT WHEN HE WAS DRIVING, HIS BLOOD GLUCOSE MONITOR STARTED SMOKING AND CAUGHT ON FIRE. THE CUSTOMER REPORTED THAT HE THREW THE DEVICE OUT THE WINDOW OF THE CAR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18146527 ↗MalfunctionJun 30, 2021Fire; Melted; Fire; Melted
THE CALLER REPORTED THAT THE BLOOD GLUCOSE METER CAUGHT ON FIRE WHILE IT WAS STILL IN THE BOX. THE CUSTOMER OBSERVED THE METER BOX IN FLAMES AND STATED FLAMES AND SMOKE WERE VISIBLE AND THAT SHE SMELLED THE METER BURNING. THE METER HOUSING NOW SHOWS VISIBLE SIGNS OF MELTING AND THE CUSTOMER'S TABLE WAS DAMAGED BY THE FIRE. THE METER WAS NEW IN BOX AND HAD NEVER BEEN USED. THE CUSTOMER STATED THAT THE METER WAS NOT EXPOSED TO ANY EXTERNAL HEAT SOURCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12092417 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under 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-1742-2026 · Feb 13, 2026 · Open, ClassifiedMiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
- Z-1739-2026 · Feb 13, 2026 · Open, ClassifiedMiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
- 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-1265-2025 · Jan 31, 2025 · Open, ClassifiedMiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
- 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-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-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-1881
- 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 SF M
- 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
- Z-0956-2020 · Nov 21, 2019 · Open, ClassifiedMedtronic MiniMed 670G System with SmartGuard, Ref #s/Model Number(s) - MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, and MM
- Z-2605-2017 · May 8, 2017 · TerminatedMiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
- Z-2604-2017 · May 8, 2017 · TerminatedMiniMed 640G Insulin Infusion Pump, Catalog No. MMT-1511, MMT-1711, MMT-1512, MMT-1712, MMT-1551, MMT-1751, MMT-1552, MMT-1752.
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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