# FDA recall Z-0233-2026

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-09-17.

## Product

Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch Allyn SureTemp Plus 692 (01692-200) thermometers

## Reason for recall

Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.

## Distribution

Distribution US nationwide, Canada and Colombia.

## Key facts

- **Recall number:** Z-0233-2026
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-09-17
- **Report date:** 2025-10-29

- **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-0233-2026

## Citation

> AI Analytics. FDA recall Z-0233-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0233-2026. Source: US FDA. Licensed CC0.

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