MiniMed 630G with SmartGuard — Class II medical device recall Z-0517-2021
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-0517-2021 |
|---|---|
| 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 | 206 |
| Model numbers | MMT-1714K, MMT-1754K, MMT-1755K |
Product
MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery of basal insulin (at user selectable rates) and administration of insulin boluses (in user selectable amounts) for the management of diabetes mellitus in persons, fourteen years of age and older, requiring insulin.
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-0517-2021. 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.