FDA Device recall Z-0107-2018
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
- FDA Device
- Class II
- ongoing
- Published 2017-11-29
On 2017-11-29 the FDA classified a Class II recall of Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T) by Medtronic, citing medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0107-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-09-10 |
| Published | 2017-11-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic |
| Distribution | n/a |
Product
Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)
Reason
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Identifiers
| code_info | Lot Numbers: 5179671 5179672 5179675 5179676 5179678 5179680 5174468 5174471 5185640 5185642 5185643 518564…Lot Numbers: 5179671 5179672 5179675 5179676 5179678 5179680 5174468 5174471 5185640 5185642 5185643 5185645 5185647 5185648 5185650 5176067 5176070 5176073 5176074 5176079 5176082 5176085 5185660 5185663 5185666 5185669 5185672 5185673 5176224 5176050 5176052 5176054 5176056 5189836 5189838 5189839 5173751 5173752 5189378 5189379 5189380 5174455 5174457 5174459 5174461 5189358 5189359 5189362 5189364 5189366 5185736 5174481 5174483 5174485 5174487 5189386 5189388 5189390 5189392 5189394 5189395 5179685 5179686 5179687 5179688 5179689 5170715 5170823 5170825 5170827 5173463 5174300 5173470 5173471 5173472 5173473 5173474 5173475 5173476 5173477 5170133 5170134 5170135 5179710 5179711 5179712 5179713 5179714 5179715 5179716 5179717 5179718 5179719 5179720 5179721 5179722 5179723 5179724 5179725 5179726 5179727 5179728 5170153 5170154 5170155 5179690 5179691 5179692 5179693 51796 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0107-2018%22
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