Baxter Healthcare Corporation recalls Sevoflurane, USP Inhalation Anesthetic 250 mL bottles, Rx only, Manufactured for Baxter Healthcare Corporation
Baxter Healthcare recalls 250mL Sevoflurane inhalation anesthetic bottles due to failed stability specifications. This could affect medication safety. Check your product details for recall.
Lower-risk recall
Failed Stability Specifications
Contact the company & request your remedy
What happened, in plain English
Baxter Healthcare is recalling 250 mL Sevoflurane inhalation anesthetic bottles that failed stability tests. This means the medication might not be safe for use as intended, potentially causing adverse effects if used improperly. Read more at govinfonow.com/recall/38641-baxter-sevoflurane-inhalation-anesthetic-recall-stability-failure-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/38641-baxter-sevoflurane-inhalation-anesthetic-recall-stability-failure-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1435-2019
Cite this page
“Baxter Sevoflurane Inhalation Anesthetic Recall: Stability Failure Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38641-baxter-sevoflurane-inhalation-anesthetic-recall-stability-failure-risk. Based on FDA recall #D-1435-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1435-2019%22&limit=1).
Why it’s dangerous
The medication failed stability specifications, meaning it may degrade over time and lose effectiveness. This could lead to improper dosing or reduced therapeutic effects during medical procedures.
Who’s affected
Prescribers and patients who have received this specific Sevoflurane inhalation anesthetic product. Healthcare professionals using the product for medical procedures are most at risk.
How to tell if you have this one
Check for 250 mL Sevoflurane inhalation anesthetic bottles with NDC 10019-651-64 and lot number S110F822, manufactured in Deerfield, IL, with an expiration date of May 31, 2021.
- Brand
Baxter Healthcare- Category
Drug
What to do — step by step
Check Product Details
Verify your Sevoflurane bottle's NDC number, lot number, and expiration date to confirm if it's affected.
Questions people ask
Is this product safe to use?
The recall indicates the product failed stability specifications, so it may not be safe for use as intended. Consult your healthcare provider for guidance.
What should I do if I have this product?
The recall does not specify a remedy, so check with your healthcare provider or Baxter Healthcare for further instructions.
How can I confirm if my product is recalled?
Look for NDC 10019-651-64, lot number S110F822, and expiration date May 31, 2021 on the product label.
Contact Baxter Healthcare
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-1435-2019 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall D-1435-2019 from Baxter Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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 #D-1435-2019 (June 13, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1435-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.