# FDA recall Z-0659-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2023-12-06.

## Product

Baxter Vascular Probe, Product Codes:    a)	7081015:  8CM, 1- 1.5 MM GLOBAL,    b)	7081520:  8CM, 1.5-2 MM GLOBAL,    c)	7082025:  8CM, 2-2.5 MM GLOBAL,    d)	7151015:  15CM, 1-1.5 MM GLOBAL,    e)	7151520:  15CM, 1.5- 2 MM GLOBAL,    f)	7152025:  15CM, 2- 2.5 MM GLOBAL,    g)	7451015:  45CM, 1- 1.5 MM GLOBAL,    h)	7451520:  45CM, 1.5- 2 MM GLOBAL,    i)	7452025:  45CM, 2- 2.5 MM GLOBAL,    j)	7081015ES:  8CM, 1-1.5 MM GLOBAL,    k)	7081520ES:   8CM, 1.5- 2 MM GLOBAL,    l)	7082025ES:   8CM, 2-2.5 MM GLOBAL,    m)	7151015ES:   15CM, 1-1.5 MM GLOBAL,    n)	7151520ES:   15CM, 1.5- 2 MM GLOBAL,    o)	7152025ES:   15CM, 2-2.5 MM GLOBAL,    p)	7451015ES:   45CM, 1-1.5 MM GLOBAL,    q)	7451520ES:   45CM, 1.5-2 MM GLOBAL,    r)	7452025ES:   45CM, 2-2.5 MM GLOBAL

## Reason for recall

Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0659-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-06
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0659-2024

## Citation

> AI Analytics. FDA recall Z-0659-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0659-2024. Source: US FDA. Licensed CC0.

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