US Drug Recall Register
Class II · Moderate risk Ongoing Initiated May 12, 2026 (4 months ago)

Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by…

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

Why it was recalled

Lack of Assurance of Sterility

What was recalled

Lidocaine HCl Injection USP, 25x5 mL, Single-Dose Ampules, Rx Only, Distributed by: Spectra Medical Devices, LLC, Wilmington, Made in S. Korea, NDC 65282-1605-1.

Recalling firm
Spectra Medical Devices, Llc
NDC code
65282-1605-1
Origin
MA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0554-2026

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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