US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 9, 2023 (3 years ago)

LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel)…

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

Why it was recalled

Product Mix-up: Incorrect Product Formulation

What was recalled

LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use Topical Syringe, 3mL syringe, 10/pack, Rx only, Carie Boyd Pharmaceuticals, 8400 Esters Blvd, Ste# 190, Irving, TX 75063, NDC73271-1003-1

Recalling firm
Right Value Drug Stores, LLC dba Carie Boyd's Prescription Shop
NDC code
73271-1003-1
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0140-2024

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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