FDA Drug Recalls

Recalls / Class II

Class IID-1860-2019

Product

Soothing Sore Relief (lidocaine) Cream, 4%, packaged in a) 1 OZ (NDC 69804-074-05), b) 2 OZ (NDC 69804-074-02), and c) 4 OZ (NDC 69804-074-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.

Affected lot / code info
Lot # 1228, Exp 06/21/2023

Why it was recalled

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

Recalling firm

Firm
Ridge Properties, LLC
Notification channel
Press Release
Type
Voluntary: Firm initiated
Address
4995 Ridge Dr NE, N/A, Salem, Oregon 97301-7475

Distribution

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

Timeline

Recall initiated
2019-08-09
FDA classified
2019-09-13
Posted by FDA
2019-09-25
Terminated
2023-07-12
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1860-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls