FDA Device recall Z-0782-2022
LINQ II Insertable Cardiac Monitor
- FDA Device
- Class II
- terminated
- Published 2022-03-23
On 2022-03-23 the FDA classified a Class II recall of LINQ II Insertable Cardiac Monitor by Medtronic Cardiac Rhythm And Heart Failure Crhf, citing devices may lose functionality due to susceptibility to moisture ingress.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0782-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-01-18 |
| Published | 2022-03-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Cardiac Rhythm And Heart Failure Crhf |
| Distribution | US |
Product
LINQ II Insertable Cardiac Monitor
Reason
Devices may lose functionality due to susceptibility to moisture ingress.
Identifiers
| code_info | 8 impacted devices with the following Serial number and GTIN 1) Serial RLB035341G (GTIN 00763000060374) 2) Serial RLB0…8 impacted devices with the following Serial number and GTIN 1) Serial RLB035341G (GTIN 00763000060374) 2) Serial RLB051224G (GTIN 00763000060374) 3) Serial RLB059666G (GTIN 00763000060374) 4) Serial RLB061064G (GTIN 00763000060374) 5) Serial RLB061812G (GTIN 00763000060381) 6) Serial RLB066367G (GTIN 00763000060374) 7) Serial RLB091638G (GTIN 00763000060374) 8) Serial RLB122769G (GTIN 00763000554002) |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0782-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.