US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 22, 2022 (4 years ago)

Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug: Testing results below the defined limit for the epinephrine portion of this product.

What was recalled

Sensorcaine-MPF (Bupivacaine HCl and Epinephrine Injection, USP) with Epinephrine 1:200,000 (as bitartrate), 0.25%, 25 mg per 10 mL (2.5 mg per mL), 10 mL Single Dose Vial (NDC 63323-468-01), packaged in 25 Single Dose Vials per tray (NDC 63323-468-17), Rx only, Fresenius Kabi, Lake Zurich, IL 60047.

Recalling firm
Fresenius Kabi USA, LLC
NDC code
63323-468-01
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0129-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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