Reported Dec 6, 2023 · Ongoing

ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor

Medtronic Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medtronic Inc. · 8200 Coral Sea St Ne · Mounds View, MN · 55112-4391

Is this the product you have?

    • ICM LNQ22 LINQ II
    • Model LNQ22
    • Insertable Cardiac Monitor
Lot codes and dates
  • GTIN 00763000060374
  • Serial Numbers

    2,714 of 2,714 codes

    • RLB088215G
    • RLB088216G
    • RLB088218G
    • RLB091019G
    • RLB034146G
    • RLB087479G
    • RLB127232G
    • RLB096039G
    • RLB086587G
    • RLB086621G
    • RLB088233G
    • RLB088236G
    • RLB088253G
    • RLB123314G
    • RLB043944G
    • RLB043960G
    • RLB064996G
    • RLB132967G
    • RLB100312G
    • RLB129506G
    • RLB100832G
    • RLB133215G
    • RLB135262G
    • RLB095554G
    • RLB085079G
    • RLB085091G
    • RLB076831G
    • RLB039020G
    • RLB039027G
    • RLB039991G
    • RLB067804G
    • RLB067902G
    • RLB068380G
    • RLB046661G
    • RLB046706G
    • RLB032307G
    • RLB051206G
    • RLB059647G
    • RLB059927G
    • RLB059929G
    • RLB057274G
    • RLB057275G
    • RLB057281G
    • RLB049542G
    • RLB049547G
    • RLB049558G
    • RLB050122G
    • RLB050400G
    • RLB135044G
    • RLB135571G
    • RLB116211G
    • RLB116212G
    • RLB116278G
    • RLB132853G
    • RLB041540G
    • RLB080621G
    • RLB128220G
    • RLB044256G
    • RLB045549G
    • RLB045551G
Amount recalled
64,739 units

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:45 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.