Medtronic MiniMed 670G insulin pumps (U.S. and O.U.S. versions) may have battery cap deterioration causing power loss. Affected units include specific model numbers and serials listed in the recall. Stop using immediately to prevent insulin pump failure.
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
Medtronic MiniMed 670G insulin pumps (U.S. and O.U.S. versions) are being recalled due to battery cap deterioration that can cause power loss and pump failure. This risk could lead to interrupted insulin delivery if the pump stops working.
The battery cap can deteriorate over time, similar to when it's not properly attached. This may cause the pump to lose power and stop working, which could interrupt insulin delivery to the user.
People with diabetes using the MiniMed 670G insulin pump (U.S. and O.U.S. versions) are most at risk. The recall affects specific model numbers and serial numbers listed in the notice.
Check if your pump has a model number starting with MMT-1580 through MMT-1782 or the serial numbers listed in the recall notice. The U.S. version has specific serial numbers starting with NG1839499H.
Immediately stop using the affected MiniMed 670G insulin pump to prevent potential power loss and insulin delivery interruption.
The battery cap may deteriorate, causing the pump to lose power and stop working, which could interrupt insulin delivery.
Check if your pump has a model number starting with MMT-1580 through MMT-1782 or the specific serial numbers listed in the recall notice.
Stop using the pump immediately and contact Medtronic MiniMed for further instructions.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1355-2022 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1355-2022 from Medtronic 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.
