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 IIModel LNQ22Insertable Cardiac Monitor
- Lot codes and dates
- GTIN 00763000060374
- Serial Numbers
2,714 of 2,714 codes
RLB088215GRLB088216GRLB088218GRLB091019GRLB034146GRLB087479GRLB127232GRLB096039GRLB086587GRLB086621GRLB088233GRLB088236GRLB088253GRLB123314GRLB043944GRLB043960GRLB064996GRLB132967GRLB100312GRLB129506GRLB100832GRLB133215GRLB135262GRLB095554GRLB085079GRLB085091GRLB076831GRLB039020GRLB039027GRLB039991GRLB067804GRLB067902GRLB068380GRLB046661GRLB046706GRLB032307GRLB051206GRLB059647GRLB059927GRLB059929GRLB057274GRLB057275GRLB057281GRLB049542GRLB049547GRLB049558GRLB050122GRLB050400GRLB135044GRLB135571GRLB116211GRLB116212GRLB116278GRLB132853GRLB041540GRLB080621GRLB128220GRLB044256GRLB045549GRLB045551G
- 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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