Recall RadarFamotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter International Inc., Baxter Healthcare Corpor…
CGMP Deviations
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- Baxter Healthcare Corporation — Deerfield, IL
- Severity
- Class II — moderate
- Reported
- September 9, 2026
- Quantity
- N/A
- Recall number
- D-0809-2026
- Status
- Ongoing
- Source
- FDA
Where it went
US Nationwide; Puerto Rico; and Chile.
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