---
title: "CRT-D DTBB1Q1 VIVA QUAD S IS4/DF1 US, Model Number DTBB1Q1; Implantable Cardi... — FDA record Z-1743-2023 | Is It on Recall"
description: "There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs)"
url: https://isitonrecall.com/recall/fda-device-z-1743-2023-crt-d-dtbb1q1-viva-quad-s-is4-df1-us-model-number-dtbb1q1-implantable-cardioverter-defibrillators/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# CRT-D DTBB1Q1 VIVA QUAD S IS4/DF1 US, Model Number DTBB1Q1; Implantable Cardioverter Defibrillators — FDA record Z-1743-2023

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 May 10, 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**: CRT-D DTBB1Q1 VIVA QUAD S IS4/DF1 US, Model Number DTBB1Q1; 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.
- **Classification**: Class I
- **Recalling firm**: Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1743-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1743-2023%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 00643169720206, Lot Serial Numbers: BLM202912H, BLM203000H, BLM202895H, BLM202965H, BLM203007H, BLM203028H, BLM203031H, BLM203063H, BLM202844H, BLM202900H, BLM203042H, BLM203014H, BLM203015H, BLM203062H, BLM202811H, BLM202838H, BLM202857H, BLM202858H, BLM202881H, BLM202923H, BLM203001H, BLM203021H, BLM202848H, BLM202878H, BLM202827H, BLM202952H, BLM203061H, BLM202909H, BLM202921H, BLM202942H, BLM202830H, BLM202850H, BLM202886H, BLM202888H, BLM202829H, BLM202911H, BLM202958H, BLM202982H, BLM203037H, BLM202945H, BLM202929H, BLM202949H, BLM202973H, BLM202828H, BLM202990H, BLM202947H, BLM202960H, BLM202854H, BLM202944H, BLM202810H, BLM202847H, BLM202862H, BLM202880H, BLM202904H, BLM202946H, BLM202974H, BLM202979H, BLM203006H, BLM203012H, BLM203040H, BLM202932H, BLM202913H, BLM202940H, BLM202842H, BLM202980H, BLM203029H, BLM203058H, BLM203065H, BLM202972H, BLM203051H, BLM202867H, BLM202948H, BLM203004H, BLM202832H, BLM202999H, BLM202885H, BLM202976H, BLM203035H, BLM203009H, BLM203024H, BLM202914H, BLM203002H, BLM202833H, BLM202983H, BLM202985H, BLM202986H, BLM202987H, BLM202988H, BLM202992H, BLM202996H, BLM203003H, BLM203005H, BLM203008H, BLM203016H, BLM203022H, BLM203043H, BLM203046H, BLM203047H, BLM203048H, BLM203049H, BLM203066H, BLM202851H, BLM202852H, BLM202866H, BLM202875H, BLM202984H, BLM203026H, BLM203054H, BLM202860H, BLM202927H, BLM202846H, BLM202943H, BLM202951H, BLM202989H, BLM202876H, BLM202825H, BLM202915H, BLM202954H, BLM202849H, BLM202836H, BLM203053H, BLM203064H, BLM203067H |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide - Worldwide Distribution

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
- [Arkansas](https://isitonrecall.com/state/arkansas/)
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- [Indiana](https://isitonrecall.com/state/indiana/)
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- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Maine](https://isitonrecall.com/state/maine/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
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- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [North Dakota](https://isitonrecall.com/state/north-dakota/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New Mexico](https://isitonrecall.com/state/new-mexico/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Vermont](https://isitonrecall.com/state/vermont/)
- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)
- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 28, 2023
- **Recall initiation date**: May 10, 2023
- **Center classification date**: Jun 16, 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-1743-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) records](https://isitonrecall.com/brand/medtronic-inc-cardiac-rhythm-and-heart-failure-crhf/)
