FDA Medical devices recall ·
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW recall
- Recall number
- Z-2982-2026
- Date
- (initiated July 13, 2026)
- Company / brand
- Medtronic MiniMed, Inc.
18000 Devonshire St, Northridge, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 257
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Model/UDI-DI Serial Numbers: MMT-1885CLW/00763000442187, 00763000974374/NG3150737H, NG3155194H, NG3151561H, NG3154693H, NG3151716H, NG3153547H, NG3153637H, NG3155407H, NG3152666H, NG3155788H, NG3081975H, NG2901117H, NG3080842H, NG3081463H, NG3153416H, NG3081894H, NG3153781H, NG3155944H, NG3081982H, NG3081525H, NG3155909H, NG3090722H, NG3154897H, NG3088436H, NG3088708H, NG3090073H, NG3155908H, NG3150720H, NG3092957H, NG3128715H, NG3128784H, NG3152774H, NG3153929H, NG3514566H, NG3150780H, NG3151290H, NG3151508H, NG3507161H, NG3508693H, NG3081976H, NG3151460H, NG3152051H, NG3152085H, NG3152344H, NG3153213H, NG3152772H, NG3155586H, NG3150786H, NG3153214H, NG3153385H, NG3151840H, NG3082019H, NG3153405H, NG3153788H, NG3153908H, NG3154527H, NG3151598H, NG2854971H, NG3155196H, NG3155202H, NG3155341H, NG3091491H, NG3155557H, NG3081498H NG3155688H, NG3155020H, NG3508565H, NG3155419H, NG3507536H, NG3091563H, NG3082036H, NG3154689H, NG3154995H, NG3508504H, NG3514345H, NG3509850H, NG3527505H, NG3514547H, NG3527469H, NG3504333H, NG3504598H, NG3505071H, NG3505220H, NG3505273H, NG3514617H, NG3506727H, NG3085044H, NG3507542H, NG3507547H, NG3514448H, NG3508303H, NG3508350H, NG3508371H, NG3514612H, NG3508511H, NG3508617H, NG3508698H, NG3508707H, NG3508757H, NG3508799H, NG3508903H, NG3509138H, NG3509295H, NG3509299H, NG3509452H, NG3509685H, NG3509689H, NG3509836H, NG3509914H, NG3509925H, NG3514375H, NG3514441H, NG3505246H, NG3505166H, NG3505283H, NG3151570H, NG3154948H, NG3514667H, NG3527165H, N
Distribution
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2982-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.