Medtronic recalls MiniMed 630G insulin pumps with missing solder battery connections that could interrupt insulin delivery. Affected models include MMT-1754K, MMT-1714K, and MMT-1755K. Check serial numbers listed in the recall notice.
Missing solder battery connection, which could interrupt power of insulin pump.
Medtronic is recalling certain MiniMed 630G insulin pumps that have a missing solder battery connection, which could interrupt insulin delivery. This poses a risk of interrupted insulin delivery for people with diabetes who rely on these pumps.
The insulin pump may lose power due to a missing solder battery connection, which could interrupt insulin delivery. This might cause blood sugar levels to rise dangerously high if the pump stops working unexpectedly.
People with diabetes who use the MiniMed 630G insulin pump system are affected. Those who have the specific model numbers listed in the recall are most at risk.
Check if your pump has model numbers MMT-1754K, MMT-1714K, or MMT-1755K. The recall includes specific serial numbers listed in the notice. These pumps were sold for continuous insulin delivery in adults aged 14 and older.
Look for the model number on your pump's label to see if it matches MMT-1754K, MMT-1714K, or MMT-1755K.
Reach out to Medtronic directly to confirm if your pump is affected and get instructions for next steps.
The recall is for a missing solder battery connection that could interrupt insulin delivery, potentially causing blood sugar levels to rise dangerously high.
Check if your pump has model numbers MMT-1754K, MMT-1714K, or MMT-1755K. The specific serial numbers are listed in the recall notice.
No, but you should check if your pump is affected and contact Medtronic for guidance. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0517-2021 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0517-2021 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.
