Medtronic recalls MiniMed 740G insulin pumps (O.U.S. version) due to battery cap deterioration causing potential power loss. Affected units have specific serial numbers; contact Medtronic for details.
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 is recalling certain MiniMed 740G insulin pumps because the battery cap can deteriorate, leading to power loss. This could cause the pump to stop working properly, which is dangerous for people who rely on insulin delivery.
The battery cap in these pumps can deteriorate over time, causing an incomplete battery circuit. This might result in the pump losing power or stopping function, which could lead to improper insulin delivery.
People with diabetes using the recalled MiniMed 740G insulin pumps (O.U.S. version) are affected. Those who have the specific serial numbers listed in the recall are most at risk.
Check if your MiniMed 740G pump has the specific serial numbers listed in the recall notice. The O.U.S. version of the pump is affected, and the serial numbers start with NG2644996H.
Look for the serial number on your pump's label to see if it matches the listed numbers in the recall.
Reach out to Medtronic for guidance on next steps if your pump is affected.
The battery cap can deteriorate, causing potential power loss and improper insulin delivery.
No, but you should check if your pump is affected and contact Medtronic for instructions.
The affected units have specific serial numbers starting with NG2644996H and listed in the recall notice.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1357-2022 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1357-2022 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.
