FDA Device recall Z-0110-2018
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
- FDA Device
- Class II
- ongoing
- Published 2017-11-29
On 2017-11-29 the FDA classified a Class II recall of Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T) 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-0110-2018 |
| 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) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
Reason
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Identifiers
| code_info | Lot Numbers: 5079672 5079674 5079675 5079697 5079698 5082268 5082622 5082773 5084125 5084460 5084464 508518…Lot Numbers: 5079672 5079674 5079675 5079697 5079698 5082268 5082622 5082773 5084125 5084460 5084464 5085187 5086974 5087586 5088981 5091305 5095068 5095069 5095177 5095195 5097241 5097967 5098225 5101297 5101624 5103311 5103312 5103409 5103888 5104247 5104632 5106185 5109341 5109702 5109707 5109788 5109789 5109790 5109791 5115440 5115456 5117215 5117935 5119233 5119933 5122173 5122398 5123224 5123228 5123253 5123254 5127870 5127932 5129136 5130064 5130084 5131255 5131853 5131854 5132018 5132951 5133982 5134548 5135127 5135128 5135176 5139007 5140383 5140384 5141588 5143411 5143418 5143983 5143984 5146890 5147485 5148153 5148887 5149493 5150551 5150591 5151310 5151829 5152526 5152962 5153937 5154653 5156088 5156857 5157422 5158190 5158191 5161065 5162223 5162250 5162886 5163245 5163931 5163949 5166387 5167139 5167818 5167819 5169320 5169321 5174510 5176569 5176581 5177287 51780 |
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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-0110-2018%22
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