Fresenius Kabi Compounding, LLC 2026-02-18 Health serious FDA
Health · FDA · Recall #FDA-D-0335-2026
thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron… Recall
Issued February 18, 2026 · Fresenius Kabi Compounding, LLC
In February 2026, Fresenius Kabi Compounding, LLC recalled the thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Lack of Assurance of Sterility
What you should do
- 1 Stop using thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Fresenius Kabi Compounding, LLC 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.
Official remedy (Voluntary):
Recall details
- Brand
- Fresenius Kabi Compounding, LLC
- Category
- Health
- Recall date
- February 18, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide.
- Recall number
- FDA-D-0335-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Fresenius Kabi Compounding, LLC has 8 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.