Medtronic MiniMed recalls 640G insulin pumps (O.U.S. Version) due to battery cap deterioration that may cause power loss. Affected units have specific serial numbers listed in the recall notice. Stop using immediately if you own one of these models.
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 640G insulin pumps (O.U.S. Version) because the battery cap can deteriorate, potentially causing the pump to lose power. This could lead to interrupted insulin delivery. If you own one of the affected units, stop using it immediately.
The battery cap in these pumps can deteriorate over time, similar to when it's not properly attached. This may cause the pump to lose power, leading to interrupted insulin delivery and potential health risks for users.
People with diabetes who use the MiniMed 640G insulin pump (O.U.S. Version) are most at risk. This recall affects specific units with the listed serial numbers.
Check if your pump has the serial numbers listed in the recall notice (e.g., NG1000091H, NG1000104H, etc.). The product is the MiniMed 640G Insulin Pump (O.U.S. Version) with specific model numbers.
If you own a MiniMed 640G Insulin Pump (O.U.S. Version) with the affected serial numbers, stop using it right away to prevent power loss.
The recall applies to MiniMed 640G Insulin Pumps (O.U.S. Version) with specific serial numbers listed in the notice.
Check if your pump has a serial number from the list provided in the recall notice (e.g., NG1000091H, NG1000104H, etc.).
The recall notice does not specify a replacement process; it only states to stop using the pump immediately.
We’ve drafted a message you can send Medtronic MiniMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1354-2022 — Medtronic MiniMed Medtronic MiniMed Hello, I own a Medtronic MiniMed that is covered by recall Z-1354-2022 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.
