RecallReported September 9, 2026
Class II recall by Baxter Healthcare Corporation
Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter Inter…
FDA's enforcement report of September 9, 2026 lists a Class II recall by Baxter Healthcare Corporation of Deerfield, IL. Product: Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx Only, Sterile Nonpyrogenic, Baxter Inter…. Status: Ongoing.
On the record
- Recalling firm
- Baxter Healthcare Corporation
- Location
- Deerfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall number
- D-0809-2026
- Product type
- Drugs
- Brand names
- FAMOTIDINE
- Generic names
- FAMOTIDINE
- Recall initiated
- 2026-08-06
- Reported by FDA
- 2026-09-09
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
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From FDA enforcement reports. The record may have changed since it was read.
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