FDA Device recall Z-0421-2024

ICM LNQ22 LINQ II, Model LNQ22

FDA Device
Class II
ongoing
Published 2023-12-06

On 2023-12-06 the FDA classified a Class II recall of ICM LNQ22 LINQ II, Model LNQ22 by Medtronic, citing 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 di….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0421-2024
Classification	Class II
Status	ongoing
Initiated	2023-11-03
Published	2023-12-06
Last updated	2026-09-13 11:56 UTC
Company	Medtronic
Distribution	PR

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.

Identifiers

code_info	GTIN 00763000060374, Serial Numbers: RLB088215G, RLB088216G, RLB088218G, RLB091019G, RLB034146G, RLB087479G, RLB127232… 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, RL

code_info

GTIN 00763000060374, Serial Numbers: RLB088215G, RLB088216G, RLB088218G, RLB091019G, RLB034146G, RLB087479G, RLB127232…

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, RL

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0421-2024%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.