Contour Plus Link 2 — Class II medical device recall Z-3201-2018
Terminated recall by Medtronic Inc., reported 2018-09-26. CONTOUR PLUS LINK 2.4 meter with an incorrect unit of measure was included into meter kits and distributed. Th
| Recall number | Z-3201-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Northridge, CA, United States |
| Recall initiated | 2018-05-16 |
| Classified | 2018-09-19 |
| Reported by FDA | 2018-09-26 |
| Terminated | 2020-06-30 |
| Countries outside the US | SK |
| Quantity | 2 |
| Lot numbers | BG1245623B, BG1245624B, MD04M051P |
| Model numbers | MMT-1151SK |
Product
Contour Plus Link 2.4, Product Catalog Number: MMT-1151SK. wireless blood glucose monitoring system Contour Plus LINK 2.4 wireless blood glucose monitoring system (glucometer, test strips and control solution) is designed for self-testing by persons with diabetes and the monitoring of glucose concentrations for quantitative glucose measurement in fresh capillary full blood removed from the user's fingertips or palms. It is only for in vitro diagnostic use.
Reason for recall
CONTOUR PLUS LINK 2.4 meter with an incorrect unit of measure was included into meter kits and distributed. This meter contains the incorrect unit of measure mg/dL instead of mmol/L.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3201-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.