LINQ II Insertable Cardiac Monitor — Class II medical device recall Z-0782-2022
Terminated recall by Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), reported 2022-03-23, distributed nationwide. Devices may lose functionality due to susceptibility to moisture ingress.
| Recall number | Z-0782-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), Mounds View, MN, United States |
| Recall initiated | 2022-01-18 |
| Classified | 2022-03-11 |
| Reported by FDA | 2022-03-23 |
| Terminated | 2026-05-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | IT |
| Quantity | 8 devices |
| UPC / GTIN / UDI-DI | 00763000060374, 00763000060381, 00763000554002 |
| Serial numbers | RLB035341G, RLB051224G, RLB059666G, RLB061064G, RLB061812G, RLB066367G, RLB091638G, RLB122769G |
Product
LINQ II Insertable Cardiac Monitor
Reason for recall
Devices may lose functionality due to susceptibility to moisture ingress.
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-0782-2022. 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.