- Recalling firm
- Medtronic MiniMed, Inc.
- Reason for recall
- Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
- Affected products (lot / model / serial)
- Model/UDI-DI/Serial Numbers: MMT-1711/00763000404550/NG2660048H, NG2663343H, NG3015306H; MMT-1712/00763000404567/NG2628486H, NG2758213H, NG2999651H, NG3349198H, NG3351719H, NG2678842H, NG2831821H, NG2831546H, NG2932027H, NG3049657H, NG3033094H, NG2831538H, NG3738739H
- Units affected
- 16
- Distribution pattern
- International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
- Firm location
- Northridge, CA, United States
- Recall type
- Voluntary: Firm initiated
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2980-2026
- Recall initiated
- July 13, 2026
- FDA classification date
- August 18, 2026
- FDA report date
- August 26, 2026
- FDA event ID
- 99374
- Last updated on HTM Vibe
- September 8, 2026