Medtronic recalls MiniMed 670G insulin pumps with specific model numbers due to potential cleaning issues causing insulin delivery errors. Affected users should contact Medtronic for details.
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.
Medtronic is recalling MiniMed 670G insulin pumps with model numbers MMT-1781 and MMT-1782. These pumps may have been cleaned with products that could cause incorrect insulin delivery, leading to dangerous blood sugar levels.
The pumps may have been cleaned with chemicals that damage internal parts, allowing moisture to enter. This can cause the pump to deliver too much or too little insulin, leading to dangerously high or low blood sugar levels.
People using MiniMed 670G insulin pumps with model numbers MMT-1781 or MMT-1782 are affected. Those with diabetes who rely on these pumps for insulin delivery are at risk.
Check your pump's model number on the device or label. The affected models are MMT-1781 and MMT-1782 with specific serial numbers listed in the recall notice.
Look for the model number on your pump's device or label to confirm if it's MMT-1781 or MMT-1782.
Reach out to Medtronic directly for guidance on next steps and potential remedies.
The affected models are MMT-1781 and MMT-1782 with specific serial numbers listed in the recall notice.
Damaged pumps could deliver incorrect insulin amounts, leading to hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
The recall does not require immediate stop use; affected users should check their model and contact Medtronic for guidance.
We’ve drafted a message you can send Medtr: MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-2981-2026 — Medtr: MiniMed Medtr: MiniMed Hello, I own a Medtr: MiniMed that is covered by recall Z-2981-2026 from Medtr: MiniMed. 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.
