RecallRadar

FDA Drug recall D-1857-2019

PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-019-14), b) 2 Oz (NDC 69804-019-15…

On 2019-09-25 the FDA classified a Class II recall of PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-019-14), b) 2 Oz (NDC 69804-019-15… by Ridge Properties, citing microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1857-2019
ClassificationClass II
Statusterminated
Initiated2019-08-09
Published2019-09-25
Last updated2026-09-13 11:52 UTC
CompanyRidge Properties
DistributionUS

Product

PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-019-14), b) 2 Oz (NDC 69804-019-15), and c) 4 Oz (NDC 69804-019-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

Reason

Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.

Identifiers

code_infoLot # 1213, Exp 06/05/2023

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1857-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.