Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles...

FDA Recall #D-0296-2022 — Class II — November 30, 2021

Recall #D-0296-2022 Date: November 30, 2021 Classification: Class II Status: Ongoing

Product Description

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

Reason for Recall

Superpotent Drug: Minimally superpotent

Recalling Firm

Teligent Pharma, Inc. — Buena, NJ

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

7,176 bottles

Distribution

Distributed to a wholesaler in CO who further distributed Nationwide in the USA

Code Information

Lot #: 15594, Exp Date 05/2023

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated