Official recall record
ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-11-03
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00763000060374
- Brand on record
- Medtronic Inc.
What the authority reported
It may create the potential for amplified noise and/or overall signal reduction of the ICM, which may interfere with intended recordings of heart rhythms. This noise pattern is different from occasional noise due to device position/migration, patient activity, or external electromagnetic interference.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
All 8 official recall notices naming Medtronic, Inc. on this site →
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