Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump
Reason for recall
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- MiniMed 780G Insulin Pump, Model: MMT-1885CLWMMT-1886CLWUDI-DI Serial259 affected lotsMMT-1885CLW/0076300044218700763000974374/NG3150737HNG3155194HNG3151561HNG3154693HNG3151716HNG3153547HNG3153637H
+251 more
NG3155407HNG3152666HNG3155788HNG3081975HNG2901117HNG3080842HNG3081463HNG3153416HNG3081894HNG3153781HNG3155944HNG3081982HNG3081525HNG3155909HNG3090722HNG3154897HNG3088436HNG3088708HNG3090073HNG3155908HNG3150720HNG3092957HNG3128715HNG3128784HNG3152774HNG3153929HNG3514566HNG3150780HNG3151290HNG3151508HNG3507161HNG3508693HNG3081976HNG3151460HNG3152051HNG3152085HNG3152344HNG3153213HNG3152772HNG3155586HNG3150786HNG3153214HNG3153385HNG3151840HNG3082019HNG3153405HNG3153788HNG3153908HNG3154527HNG3151598HNG2854971HNG3155196HNG3155202HNG3155341HNG3091491HNG3155557HNG3081498HNG3155688HNG3155020HNG3508565HNG3155419HNG3507536HNG3091563HNG3082036HNG3154689HNG3154995HNG3508504HNG3514345HNG3509850HNG3527505HNG3514547HNG3527469HNG3504333HNG3504598HNG3505071HNG3505220HNG3505273HNG3514617HNG3506727HNG3085044HNG3507542HNG3507547HNG3514448HNG3508303HNG3508350HNG3508371HNG3514612HNG3508511HNG3508617HNG3508698HNG3508707HNG3508757HNG3508799HNG3508903HNG3509138HNG3509295HNG3509299HNG3509452HNG3509685HNG3509689HNG3509836HNG3509914HNG3509925HNG3514375HNG3514441HNG3505246HNG3505166HNG3505283HNG3151570HNG3154948HNG3514667HNG3527165HNG3527243HNG3527298HNG3527468HNG3527480HNG3527491HNG3527580HNG3527529HNG3527543HNG3527571HNG3527574HNG3092722HNG3527581HNG3527611HNG3527637HNG3527642HNG3527672HNG3527710HNG3527737HNG3527760HNG3527865HNG3527918HNG3527961HNG3527989HNG3528017HNG3528023HNG3528036HNG3528061HNG3528120HNG3528147HNG3528156HNG3528158HNG3528180HNG3528218HNG3528226HNG3528378HNG3539964HNG3539969HNG3539970HNG3539999HNG3540001HNG3540013HNG3540029HNG3540046HNG3540053HNG3540084HNG3540191HNG3540270HNG3540310HNG3540320HNG3540581HNG3540604HNG3540628HNG3540629HMMT-1886CLW/0076300044219400763000974381/NG2966956HNG2970938HNG2986362HNG3013390HNG3057910HNG3167493HNG3466128HNG3098147HNG3136398HNG3137113HNG3139432HNG3143920HNG3144721HNG3145486HNG3145488HNG3471528HNG3167609HNG3147120HNG3147035HNG3430059HNG3438451HNG3464758HNG3163796HNG3166778HNG3409587HNG3167450HNG3167623HNG3167967HNG3169694HNG3170253HNG3321081HNG3409583HNG3409611HNG3409656HNG3409680HNG3409697HNG3409716HNG3409807HNG3409825HNG3409831HNG3409854HNG3409925HNG3409959HNG3410005HNG3410053HNG3410092HNG3410111HNG3410166HNG3410189HNG3410227HNG3410233HNG3410243HNG3410279HNG3410304HNG3410389HNG3410398HNG3429103HNG3429377HNG3429485HNG3429881HNG3430107HNG3430448HNG3437945HNG3437957HNG3438394HNG3470788HNG3466185HNG3466619HNG3466620HNG3467368HNG3467586HNG3468759HNG3469430HNG3469907HNG3470728HNG3168104HNG3472157HNG3169669HNG3170079HNG3430111HNG3429099HNG3437621HNG3167969HNG3465813HNG3167397H
What the firm is doing
On 7/13/2026, field safety notices were sent to customers asking them to do the following: 1) Stop using the loaner pump and contact the firm to arrange for loaner pump return. 2) Contact your Healthcare Professional (HCP) to ensure you have access to backup insulin therapy supplies or alternative plans, which may include short- and long-acting insulins, syringes, with dosage instructions from your HCP. 3) Complete and return the customer acknowledgement form. Questions can be directed to the firm's Tech Support: 1-800-646-4633
DistributionShow detailsHide
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2982-2026
- FDA 510(k) clearance · K251032The device's official FDA premarket clearance record
- FDA device classification · QFGOfficial FDA classification for this device type
- CFR regulation · 21 CFR 880.5730The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Medtronic MiniMed, Inc.Search for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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