FDA Device recall Z-1770-2023

CRTD DTMC1QQ COMPIA MRI QUAD US DF4, Model Number DTMC1QQ

FDA Device
Class I
ongoing
Published 2023-06-28

On 2023-06-28 the FDA classified a Class I recall of CRTD DTMC1QQ COMPIA MRI QUAD US DF4, Model Number DTMC1QQ 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

Agency	FDA Device
Recall number	Z-1770-2023
Classification	Class I
Status	ongoing
Initiated	2023-05-10
Published	2023-06-28
Last updated	2026-09-13 11:56 UTC
Company	Medtronic Cardiac Rhythm And Heart Failure Crhf
Distribution	US

Product

CRTD DTMC1QQ COMPIA MRI QUAD US DF4, Model Number DTMC1QQ; 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 00643169720749, Lot Serial Numbers: RPL202320H, RPL202797H, RPL202825H, RPL203304H, RPL203279H, RPL203319H, RPL20… GTIN 00643169720749, Lot Serial Numbers: RPL202320H, RPL202797H, RPL202825H, RPL203304H, RPL203279H, RPL203319H, RPL203730H, RPL203754H, RPL204075H, RPL202479H, RPL202565H, RPL202842H, RPL203342H, RPL203518H, RPL203521H, RPL203522H, RPL203534H, RPL203543H, RPL203556H, RPL203602H, RPL203718H, RPL203723H, RPL203785H, RPL203210H, RPL202222H, RPL202318H, RPL202555H, RPL202697H, RPL202831H, RPL203172H, RPL202156H, RPL202223H, RPL202514H, RPL203290H, RPL203308H, RPL203446H, RPL202803H, RPL202347H, RPL202465H, RPL202684H, RPL202688H, RPL202707H, RPL202934H, RPL202972H, RPL203031H, RPL203078H, RPL203345H, RPL203399H, RPL203581H, RPL203623H, RPL203688H, RPL202382H, RPL202497H, RPL202590H, RPL203217H, RPL203225H, RPL203363H, RPL203369H, RPL203428H, RPL203479H, RPL203480H, RPL203484H, RPL203487H, RPL203488H, RPL203500H, RPL203513H, RPL203569H, RPL203794H, RPL202376H, RPL202499H, RPL202905H, RPL202940H, RPL203030H, RPL203784H, RPL203795H, RPL203957H, RPL202146H, RPL202538H, RPL202681H, RPL202892H

code_info

GTIN 00643169720749, Lot Serial Numbers: RPL202320H, RPL202797H, RPL202825H, RPL203304H, RPL203279H, RPL203319H, RPL20…

GTIN 00643169720749, Lot Serial Numbers: RPL202320H, RPL202797H, RPL202825H, RPL203304H, RPL203279H, RPL203319H, RPL203730H, RPL203754H, RPL204075H, RPL202479H, RPL202565H, RPL202842H, RPL203342H, RPL203518H, RPL203521H, RPL203522H, RPL203534H, RPL203543H, RPL203556H, RPL203602H, RPL203718H, RPL203723H, RPL203785H, RPL203210H, RPL202222H, RPL202318H, RPL202555H, RPL202697H, RPL202831H, RPL203172H, RPL202156H, RPL202223H, RPL202514H, RPL203290H, RPL203308H, RPL203446H, RPL202803H, RPL202347H, RPL202465H, RPL202684H, RPL202688H, RPL202707H, RPL202934H, RPL202972H, RPL203031H, RPL203078H, RPL203345H, RPL203399H, RPL203581H, RPL203623H, RPL203688H, RPL202382H, RPL202497H, RPL202590H, RPL203217H, RPL203225H, RPL203363H, RPL203369H, RPL203428H, RPL203479H, RPL203480H, RPL203484H, RPL203487H, RPL203488H, RPL203500H, RPL203513H, RPL203569H, RPL203794H, RPL202376H, RPL202499H, RPL202905H, RPL202940H, RPL203030H, RPL203784H, RPL203795H, RPL203957H, RPL202146H, RPL202538H, RPL202681H, RPL202892H

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-1770-2023%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.