FDA Device recall Z-0517-2021
MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery o…
- FDA Device
- Class II
- ongoing
- Published 2020-12-09
On 2020-12-09 the FDA classified a Class II recall of MiniMed 630G with SmartGuard, insulin pump, Ref/Model # MMT-1754K, MMT-1714K, MMT-1755K - Product Usage: intended for continuous delivery o… by Medtronic, citing missing solder battery connection, which could interrupt power of insulin pump.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0517-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-04-30 |
| Published | 2020-12-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medtronic |
| Distribution | US |
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
Missing solder battery connection, which could interrupt power of insulin pump.
Identifiers
| code_info | All serial numbers; expiration date- 3 years from date of manufacture. NG2094617H NG2094618H NG2094623H NG2094625H NG…All serial numbers; expiration date- 3 years from date of manufacture. NG2094617H NG2094618H NG2094623H NG2094625H NG2094627H NG2094628H NG2094629H NG2094631H NG2094632H NG2094634H NG2094635H NG2094636H NG2094637H NG2094638H NG2094639H NG2094640H NG2094641H NG2094642H NG2094644H NG2094645H NG2094646H NG2094647H NG2094648H NG2094649H NG2094650H NG2094651H NG2094652H NG2094653H NG2094654H NG2094655H NG2094656H NG2094657H NG2094658H NG2094659H NG2094660H NG2094661H NG2094662H NG2094663H NG2094664H NG2094668H NG2094669H NG2094670H NG2094695H NG2094696H NG2094697H NG2094698H NG2094699H NG2094700H NG2094702H NG2094704H NG2094705H NG2094707H NG2094711H NG2094712H NG2094714H NG2094718H NG2094719H NG2094724H NG2094726H NG2094728H NG2094730H NG2094732H NG2094733H NG2094735H NG2094737H NG2094739H NG2094740H NG2094743H NG2094767H NG2094769H NG2094771H NG2094772H NG2094773H NG2094774H NG2094775H NG2094776H NG2094777H NG2094779H NG2094781H NG2094783H NG2094789H NG2094795H NG2094799H NG2094800H NG2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0517-2021%22
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