MiniMed 670G — Class II medical device recall Z-0516-2021
Ongoing recall by Medtronic Inc., reported 2020-12-09, distributed nationwide. Missing solder battery connection, which could interrupt power of insulin pump.
| Recall number | Z-0516-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Northridge, CA, United States |
| Recall initiated | 2020-04-30 |
| Classified | 2020-12-02 |
| Reported by FDA | 2020-12-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, NL, NO |
| Quantity | 391 |
| Model numbers | MMT-1760KPK, MMT-1762KCN, MMT-1762WWK |
Product
MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous or periodic monitoring of glucose levels in the fluid under the skin, and detecting possible low and high glucose episodes. When using a sensor and transmitter, the pump displays continuous sensor glucose values and stores this data so that it can be analyzed to track patterns and improve diabetes management. This data can be uploaded to a computer for analysis of historical glucose values.
Reason for recall
Missing solder battery connection, which could interrupt power of insulin pump.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0516-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.