Skip to content
Recall Observatory FDA recall evidence

Drug product

Superior Pain & Itch Relief (lidocaine) Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-073-14), b) 2 Oz (NDC 69804-073-15), and c) 4 Oz (NDC 69804-073-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

D-1859-2019

August 09, 2019

Class II

Product summary

Firm
Ridge Properties, LLC
Event
Event 83538
Status
Terminated
Classification
Class II
Quantity
109.64 ounces total
Official record key
drug-enforcement:D-1859-2019

Official wording

Reason: Superpotent Drug: products were found to be contaminated and above specification for lidocaine assay.

Code information: Lot # 1213, Exp 06/05/2023

Distribution pattern: Nationwide in the USA via internet sales through Amazon.com; ebay.com; Walmart.com; tatbalm.net; Naturallyhl.com

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Superpotent