FDA Device recall Z-0518-2021
MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of i…
- FDA Device
- Class II
- ongoing
- Published 2020-12-09
On 2020-12-09 the FDA classified a Class II recall of MiniMed 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of i… 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-0518-2021 |
| 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 640G, insulin pump, Ref/Model # MMT-1711K, MMT-1752K, MMT-1752, Rx Only - Product Usage: indicated for the continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons 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: NG2095284H, NG2095319H |
|---|
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-0518-2021%22
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