Medtronic Minimally Invasive Therapies Group recalls
Medtronic Minimally Invasive Therapies Group has 2 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 21 Mar 2018.
Total recalls2since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 21 Mar 2018
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why medtronic minimally invasive therapies group is recalled
Product types
By year
All medtronic minimally invasive therapies group recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Argyle Suction Tubing (Product # 8888301515) Argyle Suction recalled | Medtronic Minimally Invasive Therapies Group | Labeling Errors | Nationwide |
| Device | CLASS II | Mahurkar"* Elite Acute Dual Lumen Dialysis Catheter recalled | Medtronic Minimally Invasive Therapies Group | Other | MA |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.