US Drug Recall Register
Class III · Low risk Terminated Initiated Jul 29, 2021 (5 years ago)

Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Viscosity Specifications: lot does not meet specification for Viscosity, which was determined through routine testing.

What was recalled

Lidocaine Ointment USP, 5% Rx Only, Net Wt 35.44 g(1 1/4 oz)packaged in a laminat tube, Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-008-14.

Recalling firm
Teligent Pharma, Inc.
NDC code
52565-008-14
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0785-2021

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.

Other Lidocaine recalls

See all