PlainRecalls

Medtronic MiniMed

24 recalls on record · Latest: Jan 11, 2023

Medtronic MiniMed Recall Insight

Medtronic MiniMed appears on 24 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.029% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jan 11, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 24 entries, severity tagging shows 1 critical, 23 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 24 of 24 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (24). The date window on this page runs from Apr 17, 2013 to Jan 11, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Jan 11, 2023

Guardian iOS app (MMT-8200) and Guardian Android app (MMT-8201), part of the Guardian 4 system

FDA Devices Moderate Nov 16, 2022

Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711, MMT-1712, MMT-1751, MMT-1752

FDA Devices Moderate Nov 16, 2022

Insulin 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…

FDA Devices Moderate Jul 20, 2022

MiniMed 640G Insulin Pump (O.U.S. Version)

FDA Devices Moderate Jul 20, 2022

MiniMed 740G Insulin Pump (O.U.S. Version)

FDA Devices Moderate Jul 20, 2022

MiniMed 670G Insulin Pump (U.S. and O.U.S. Version)

FDA Devices Moderate Jul 20, 2022

MiniMed 720G Insulin Pump (O.U.S. Version)

FDA Devices Moderate Jul 20, 2022

MiniMed 780G Insulin Pump (O.U.S. Version)

FDA Devices Moderate Jul 20, 2022

MiniMed 770G Insulin Pump (U.S. and O.U.S. Version)

FDA Devices Moderate Jun 9, 2021

MiniMed 670G Insulin Pump: Models: PUMP MMT-1740KX 670G V6.3 SF MG CLIN;¿ PUMP MMT-1740KX 670G V6.3 CLIN 020 MG;¿ PUMP MMT-1741KFX 670G V6.3 SF M…

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model number MMT-723

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model number MMT-523K

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model numbers MMT 515 and MMT-715

FDA Devices Moderate Apr 1, 2020

MiniMed Insulin Pump, model # MMT-508

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model number MMT-522

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Veo Insulin pump, model numbers MMT-554 and MMT-754

FDA Devices Moderate Apr 1, 2020

MiniMed Paradigm 512 Insulin pump

FDA Devices Moderate Apr 1, 2020

MiniMed Paradigm Insulin pump, model number MMT-712

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model number MMT-712E

FDA Devices Moderate Apr 1, 2020

MiniMed Paradigm Model 511 Insulin Pump

FDA Devices Moderate Apr 1, 2020

Medtronic MiniMed Paradigm Insulin pump, model number MMT-722

FDA Devices Moderate Aug 28, 2013

Medtronic MiniMed Paradigm Reservoirs, Model No: MMT-326A (1.8mL) and MMT-332A (3.0mL) The model MMT-326A and MMT-332A are syringe type insulin re…

FDA Devices Critical Jul 17, 2013

Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets are intended for use with Paradigm insulin infusion pumps.

FDA Devices Moderate Apr 17, 2013

Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds