Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor… — Class II medical device recall Z-2076-2021
Ongoing recall by Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), reported 2021-07-21, distributed nationwide. Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's after a ride-through POR reset.
| Recall number | Z-2076-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF), Mounds View, MN, United States |
| Recall initiated | 2021-05-14 |
| Classified | 2021-07-14 |
| Reported by FDA | 2021-07-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, CA, CH, DE, DK, FI, GB, IE, IT, NL, SE |
| Quantity | 21,685 |
| Model numbers | LNQ22 |
Product
Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
Reason for recall
Device fail to detect Brady episodes, Pause (Asystole) episodes and PVC's after a ride-through POR reset.
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-2076-2021. 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.