Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690… Recall
Issued October 29, 2025 · Baxter Healthcare Corporation
In October 2025, Baxter Healthcare Corporation recalled the Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Baxter Healthcare Corporation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- Baxter Healthcare Corporation
- Category
- Health
- Recall date
- October 29, 2025
- Units affected
- Not reported
- Sold at
- Distribution US nationwide, Canada and Colombia.
- Recall number
- FDA-Z-0233-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Baxter Healthcare Corporation has 36 recalls in our database, including 5 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.