US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 29, 2018 (8 years ago)

Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use…

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

Why it was recalled

Subpotent Drug: Stability data does not support the current expiration dating of 55 days after compounding.

What was recalled

Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic Use (Concentration=10 mg/mL) 0.25 mL Total Volume, Rx only , SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205 877-550-5059

Recalling firm
SCA Pharmaceuticals
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0918-2018

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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