Oral Probe — Class II medical device recall Z-0233-2026
Ongoing recall by Baxter Healthcare Corporation, reported 2025-10-29, distributed nationwide. Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected prob
| Recall number | Z-0233-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-09-17 |
| Classified | 2025-10-23 |
| Reported by FDA | 2025-10-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO |
| Quantity | 5,209 |
| Serial numbers | 24518445, 24518446, 24518447, 24518448, 24518449, 24518450, 24518451, 24518452, 24518453, 24518454, 24518455, 24518456, 24518457, 24518458, 24518459, 24518460, 24518461, 24518462, 24518463, 24518464, 24518465, 24518466, 24518467, 24518468, 24518469 and 475 more |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0233-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.