RecallRadar

FDA Device recall Z-1734-2023

CRTD VIVA QUAD XT CUST PARY GOLD, Model Number DTBA1QQPG

On 2023-06-28 the FDA classified a Class I recall of CRTD VIVA QUAD XT CUST PARY GOLD, Model Number DTBA1QQPG by Medtronic Cardiac Rhythm And Heart Failure Crhf, citing there is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynch….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1734-2023
ClassificationClass I
Statusongoing
Initiated2023-05-10
Published2023-06-28
Last updated2026-09-13 11:56 UTC
CompanyMedtronic Cardiac Rhythm And Heart Failure Crhf
DistributionUS

Product

CRTD VIVA QUAD XT CUST PARY GOLD, Model Number DTBA1QQPG; Implantable Cardioverter Defibrillators

Reason

There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, including currently available ICDs and CRT-Ds.

Identifiers

code_info
GTIN 00643169968585, Lot Serial Numbers: BLC229283H, BLC229226H, BLC229270H, BLC229280H, BLC229229H, BLC228997H, BLC22…GTIN 00643169968585, Lot Serial Numbers: BLC229283H, BLC229226H, BLC229270H, BLC229280H, BLC229229H, BLC228997H, BLC229238H, BLC229043H, BLC229231H, BLC229046H, BLC229045H, BLC229230H, BLC228995H, BLC229010H

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-1734-2023%22

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