Fresenius Kabi USA, LLC: Famotidine Injection, USP, 20 mg per 2 mL (10 mg per
Recall reason: Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.. Recalled by Fresenius Kabi USA, LLC. Distribution: Nationwide within the United States as well as AK, HI, and PR.. Classification (Class I — serious health hazard). Affected lots/NDC/dates: Lot #: 6133156, 6133194, Exp Date: 08/2026; 6133388, Exp Date: 10/2026.. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
📬 Get email alerts for new Product Recalls & Refunds
Free — we'll email you when new matching opportunities appear. No spam, unsubscribe anytime.
New here? Here's how Reward Opportunity works:
🔔 More Product Recalls & Refunds
Product recalls offering refunds, replacements, or repairs to consumers who purchased the item.
Browse all product recalls & refunds →Not just this one — find everything you qualify for
Our AI scans 8,000+ bounties, settlements, grants, recalls, and paid studies against your profile to rank what you can actually claim.
Get My Free Match Report