Recall of Medtronic MiniMed 780G Insulin Pumps (O.U.S. Version) due to battery cap deterioration causing potential power loss. Affected units have specific serial numbers and UDI codes listed in the recall notice.
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 780G insulin pumps (O.U.S. Version) because the battery cap can deteriorate, leading to power loss and potential interruption of insulin delivery. This could cause dangerous blood sugar fluctuations for users.
The battery cap in these pumps can deteriorate over time, which may cause the pump to lose power or stop working properly. This could lead to interruptions in insulin delivery, potentially causing dangerous blood sugar levels.
People with diabetes who use the MiniMed 780G insulin pump (O.U.S. Version) are affected. Those who have the specific serial numbers or UDI codes listed in the recall are most at risk.
Check if your pump has the product number/CFN (O.U.S. Version) MiniMed 780G (MMT-1884 to MMT-1896, etc.) or the UDI codes listed in the recall notice. The specific serial numbers are provided in the official recall list.
Look for the product number/CFN (O.U.S. Version) on your pump, which should be one of the listed codes (e.g., MMT-1884, MMT-1885, etc.).
If your pump is affected, contact Medtronic directly for instructions on how to return or replace the pump.
The battery cap in these pumps can deteriorate over time, which may cause the pump to lose power or stop working properly, leading to interruptions in insulin delivery.
Check if your pump has the product number/CFN (O.U.S. Version) MiniMed 780G (MMT-1884 to MMT-1896, etc.) or the UDI codes listed in the recall notice.
Contact Medtronic directly for instructions on how to return or replace the pump.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1359-2022 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1359-2022 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.
