Medtronic recalls MiniMed Mio (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T) infusion sets with potential for over-delivery of insulin. Lot numbers listed in the recall.
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Medtronic is recalling certain MiniMed Mio insulin infusion sets that may deliver too much insulin. This could cause dangerous blood sugar levels. Affected units have specific model numbers and lot numbers listed in the recall.
The infusion sets have a potential for over-delivery of insulin, which could lead to dangerously low blood sugar levels. This risk occurs due to a malfunction in the insulin delivery mechanism.
People using Medtronic MiniMed Mio insulin pumps with the listed model numbers and lot numbers are affected. Those with diabetes who rely on these pumps are most at risk.
Check your MiniMed Mio pump model number (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T) and lot number against the list provided in the recall.
Compare your pump's model number and lot number with the list provided in the recall to see if it's affected.
The infusion sets have the potential for over-delivery of insulin, which could cause dangerously low blood sugar levels.
Check your pump's model number (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T) and lot number against the list provided in the recall.
The recall does not specify a remedy, so you should contact Medtronic directly for further instructions.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0110-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0110-2018 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
