---
title: "HVI CARDIAC ROBOT PACK. Medical convenience kit. — FDA record Z-2252-2025 | Is It on Recall"
description: "CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration."
url: https://isitonrecall.com/recall/fda-device-z-2252-2025-hvi-cardiac-robot-pack-medical-convenience-kit/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# HVI CARDIAC ROBOT PACK. Medical convenience kit. — FDA record Z-2252-2025

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 Jun 11, 2025. 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**: HVI CARDIAC ROBOT PACK. Medical convenience kit.
- **Reason**: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- **Classification**: Class II
- **Recalling firm**: AVID Medical, Inc.
- **Quantity**: 20 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2252-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2252-2025%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 | Model No. RYCB72-04; UDI: 10809160434666; Kit Lot No. 1625487. |

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

## Distribution

Domestic: CA, IL, MD, OH, PA, TX, WA.

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

- [California](https://isitonrecall.com/state/california/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Aug 13, 2025
- **Recall initiation date**: Jun 11, 2025
- **Center classification date**: Aug 4, 2025

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-2252-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [AVID Medical, Inc. records](https://isitonrecall.com/brand/avid-medical-inc/)