--- title: "ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor — FDA record Z-0421-2024 | Is It on Recall" description: "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" url: https://isitonrecall.com/recall/fda-device-z-0421-2024-icm-lnq22-linq-ii-model-lnq22-insertable-cardiac-monitor/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor — FDA record Z-0421-2024 Reported ongoing Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Nov 3, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: ICM LNQ22 LINQ II, Model LNQ22; Insertable Cardiac Monitor - **Reason**: 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. - **Classification**: Class II - **Recalling firm**: Medtronic Inc. - **Quantity**: 64,739 units - **Agency-reported status**: Ongoing - **Source record identifier**: Z-0421-2024 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2024%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | GTIN 00763000060374, Serial Numbers: 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, RLB131768G, RLB067275G, RLB067283G, RLB076103G, RLB097835G, RLB123630G, RLB123632G, RLB123637G, RLB124673G, RLB073925G, RLB079721G, RLB082968G, RLB090643G, RLB047705G, RLB050161G, RLB051708G, RLB071194G, RLB074924G, RLB040742G, RLB040745G, RLB040747G, RLB042297G, RLB042305G, RLB126760G, RLB049893G, RLB056158G, RLB060723G, RLB067531G, RLB072387G, RLB077136G, RLB081270G, RLB074296G, RLB074299G, RLB074311G, RLB079205G, RLB079211G, RLB079220G, RLB081471G, RLB079130G, RLB079191G, RLB075572G, RLB075573G, RLB075791G, RLB046637G, RLB046831G, RLB046834G, RLB046839G, RLB046842G, RLB064638G, RLB064714G, RLB064723G, RLB064727G, RLB064729G, RLB072023G, RLB072026G, RLB072042G, RLB072045G, RLB073339G, RLB046700G, RLB046701G, RLB046707G, RLB046708G, RLB061262G, RLB061263G, RLB061471G, RLB062138G, RLB062262G, RLB067104G, RLB067110G, RLB067140G, RLB068189G, RLB069163G, RLB054816G, RLB054863G, RLB054781G, RLB054783G, RLB054785G, RLB059008G, RLB059009G, RLB062338G, RLB062068G, RLB062077G, RLB062079G, RLB062084G, RLB062085G, RLB062149G, RLB062150G, 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RLB093904G, RLB093905G, RLB070484G, RLB070486G, RLB070487G, RLB071455G, RLB071459G, RLB064967G, RLB065796G, RLB057331G, RLB057332G, RLB057439G, RLB058975G, RLB126522G, RLB124044G, RLB077632G, RLB067265G, RLB051812G, RLB075274G, RLB076318G, RLB074081G, RLB075093G, RLB067748G, RLB051888G, RLB051981G, RLB047298G, RLB042650G, RLB036137G, RLB036140G, RLB036145G, RLB036146G, RLB036195G, RLB099384G, RLB100041G, RLB099306G, RLB130029G, RLB085599G, RLB086130G, RLB093010G, RLB096749G, RLB123693G, RLB062416G, RLB073762G, RLB129136G, RLB127179G, RLB044817G, RLB044628G, RLB123328G, RLB050974G, RLB049549G, RLB082206G, RLB082002G, RLB088970G, RLB085273G, RLB090100G, RLB073935G, RLB080273G, RLB076627G, RLB080325G, RLB079204G, RLB074559G, RLB074561G, RLB065024G, RLB065027G, RLB065029G, RLB065154G, RLB065156G, RLB068267G, RLB068271G, RLB069199G, RLB069208G, RLB067120G, RLB070512G, RLB070523G, RLB070525G, RLB047067G, RLB054926G, RLB054970G, RLB056196G, RLB059104G, RLB117929G, RLB123077G, RLB123081G, RLB123085G, RLB073760G, RLB110454G, RLB117925G, RLB121560G, RLB039535G, RLB041936G, RLB131568G, RLB131576G, RLB131595G, RLB082799G, RLB082802G, RLB082804G, RLB082808G, RLB084904G, RLB084909G, RLB084910G, RLB085782G, RLB087221G, RLB08729... | The agency lot list is longer than this excerpt. [Read the complete list at the official source](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2024%22). Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution US and Australia, Austria, Belgium, Brunei Darussalam, Canada, Czech Republic, Denmark, Finland, France, Germany, Greece, Hong Kong, Iceland, Ireland, Israel, Italy, Japan, Liechtenstein, Luxembourg, Macao, Malaysia, Netherlands, New Zealand, Northern Ireland, Norway, Portugal, Puerto Rico, Saudi Arabia, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, United Arab Emirates, United Kingdom No US distribution state could be established from this record. Check the official notice. ## Dates in the source - **Report date**: Dec 6, 2023 - **Recall initiation date**: Nov 3, 2023 - **Center classification date**: Nov 30, 2023 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0421-2024%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Inc records](https://isitonrecall.com/brand/medtronic-inc/)