MiniMed 670G Insulin Infusion Pump
Medical device recall Z-2605-2017. Published in FDA’s Enforcement Report on Jun 28, 2017.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jun 28, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Not named no state, in where it went
- 117,239 pumps how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Medtronic MiniMed is recalling the MiniMed 600 series insulin pump because it may become temporarily stuck, and the keypad becomes unresponsive.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MiniMed 670G Insulin Infusion Pump, Catalog No. MMT-1580, MMT-1780, MMT-1782, MMT-1760.
117,239 pumps, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial Number for MMT-1580 NG1008774U NG1008781U NG1008787U NG1008795U NG1008804U NG1008814U NG1008817U NG1008818U NG1008838U NG1008871U NG1008872U NG1008877U NG1008885U NG1008886U NG1008899U NG1008901U NG1008902U NG1008915U NG1008916U…
Every code shown here, 1,990 characters
Serial Number for MMT-1580 NG1008774U NG1008781U NG1008787U NG1008795U NG1008804U NG1008814U NG1008817U NG1008818U NG1008838U NG1008871U NG1008872U NG1008877U NG1008885U NG1008886U NG1008899U NG1008901U NG1008902U NG1008915U NG1008916U NG1008799U NG1008806U NG1008834U NG1008906U Serial Number for MMT-1780 NG1014265U NG1014274U NG1014275U NG1014279U NG1014270U NG1014285U NG1014286U NG1014271U NG1014264U NG1014267U NG1014289U NG1014684U NG1014682U NG1014604U NG1014650U NG1014651U NG1014613U NG1014620U NG1014639U NG1014616U NG1014618U NG1014631U NG1014636U NG1014659U NG1014605U NG1014634U NG1014665U NG1014633U NG1014662U NG1014660U NG1014624U NG1014623U NG1014610U NG1014622U NG1014635U NG1014637U NG1014640U NG1014654U NG1014661U NG1014666U NG1016855U NG1016985U NG1016976U NG1016984U NG1016978U NG1016989U NG1016966U NG1016990U NG1016975U NG1016982U NG1016967U NG1016979U NG1016812U NG1016973U NG1016969U NG1016971U NG1016974U NG1016977U NG1016981U NG1016986U NG1016987U NG1016988U NG1229998H NG1016968U NG1016972U NG1016980U NG1016983U NG1017018U NG1017020U NG1017021U NG1017023U NG1017024U NG1017027U NG1017036U NG1017037U NG1017038U NG1017040U NG1229921H NG1229913H NG1229925H NG1229904H NG1229929H NG1229922H NG1230901H NG1230088H NG1230127H NG1230210H NG1230212H NG1230885H NG1230217H NG1230899H NG1230146H NG1230149H NG1230148H NG1230175H NG1230887H NG1230160H NG1230220H NG1230037H NG1230011H NG1229936H NG1230049H NG1230019H NG1230036H NG1230097H NG1230007H NG1230084H NG1230018H NG1229933H NG1230151H NG1230169H NG1230044H NG1230014H NG1230195H NG1230888H NG1229901H NG1229994H NG1229918H NG1230150H NG1230206H NG1230893H NG1230890H NG1230078H NG1230129H NG1230201H NG1230004H NG1229932H NG1230062H NG1229961H NG1229939H NG1230209H NG1230131H NG1229916H NG1230176H NG1229973H NG1229963H NG1230110H NG1230061H NG1230106H NG1230020H NG1230138H NG1230087H NG1229912H NG1230000H NG1230192H NG1230008H NG1230050H NG1230191H NG1230024H NG1230167H NG1230076H NG1230039H NG1229907H…
FDA’s list runs to 135,796 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
US and OUS Angola Aruba Australia/NZ Austria Bahamas Bahrain Bangladesh Belgium Bolivia Botswana Bulgaria Cayman Islands Colombia Costa Rica Croatia Cyprus Czech Republic Denmark Dominican Republic El Salvador Estonia Faroe Islands Finland France Germany Greece Guadeloupe Guatemala Hong Kong Hungary Iceland India Iraq Ireland Israel Italy Japan Jordan Kazakhstan Kenya Korea Kuwait Latvia Lebanon Liechtenstein Lithuania Luxembourg Macedonia Malaysia Martinique Mauritius Morocco Namibia Nepal Netherlands New Caledonia Norway Oman Panama Paraguay Philippines Poland Portugal Qatar Reunion Romania San Marino Saudi Arabia Singapore Slovakia Slovenia South Africa Spain Sweden Switzerland Tanzania Thailand Trinidad and Tobago Turkey United Arab Emirates United Kingdom
These words name no state.
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on May 8, 2017.
- FDA classified it on Jun 20, 2017.
- FDA’s Enforcement Report published it on Jun 28, 2017.
- FDA terminated it on Jan 20, 2021.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Medtronic Inc., of Northridge, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 135,796 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
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U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.