Baxter Healthcare Corporation - Product Codes and Serial Numbers
Baxter Healthcare Corporation product codes and serial numbers for various medical devices and equipment.
Lower-risk 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.
Contact the company
What happened, in plain English
Baxter Healthcare Corporation is a leading manufacturer of medical devices and equipment. This page lists product codes and serial numbers for their various products, including the Product code 01690-400 with serial numbers ranging from 24521201 to 25047504. Read more at govinfonow.com/recall/51276-baxter-healthcare-corporation-product-codes-and-serial-numbers.
Source Summary by GovInfoNow · govinfonow.com/recall/51276-baxter-healthcare-corporation-product-codes-and-serial-numbers · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0233-2026
Cite this page
“Baxter Healthcare Corporation - Product Codes and Serial Numbers.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51276-baxter-healthcare-corporation-product-codes-and-serial-numbers. Based on FDA recall #Z-0233-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0233-2026%22&limit=1).
Why it’s dangerous
Low risk - This information is for reference and educational purposes only. It does not pose a direct threat to health or safety.
Who’s affected
Patients, healthcare providers, and medical device users
How to tell if you have this one
Product codes and serial numbers for Baxter Healthcare Corporation medical devices
- Brand
Baxter Healthcare Corporation- Category
Medical device
What to do — step by step
1
Verify the product code and serial number with the manufacturer or healthcare provider.
2
Check the product's specifications and safety information.
3
Ensure proper use and maintenance of the medical device.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Distribution US nationwide, Canada and Colombia.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 42 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0233-2026 (September 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0233-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.