RecallRadar

FDA Device recall Z-1496-2022

Merlin 2 PCS MER37000 programmer Model MER3400 software

On 2022-08-10 the FDA classified a Class II recall of Merlin 2 PCS MER37000 programmer Model MER3400 software by St Jude Medical Cardiac Rhythm Management Division, citing the Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical device….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1496-2022
ClassificationClass II
Statusongoing
Initiated2022-06-17
Published2022-08-10
Last updated2026-09-13 11:56 UTC
CompanySt Jude Medical Cardiac Rhythm Management Division
DistributionAK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY

Product

Merlin 2 PCS MER37000 programmer Model MER3400 software

Reason

The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical devices during implant and follow-up.

Identifiers

code_infoSoftware Model MER3400 v1.1.2 rev 1 or earlier.; UDI/DI 05415067037121

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-1496-2022%22

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