Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection Recalled by Fresenius Kabi USA, LLC Due to Subpotent Drug: Low out-of-specification assay results for the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Fresenius Kabi USA, LLC directly.
Affected Products
Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection, USP), 0.5%, 150 mg per 30 mL (5 mg per mL), 30 mL Single Dose Vial (NDC 63323-462-01), packaged as 25 Single Dose Vials per tray (NDC 63323-462-37), Rx only, Fresenius Kabi, Lake Zurich, IL 60047.
Quantity: 4411 trays
Why Was This Recalled?
Subpotent Drug: Low out-of-specification assay results for the epinephrine component.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Fresenius Kabi USA, LLC
Fresenius Kabi USA, LLC has 67 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report