PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4%, packaged in a) 1 OZ (NDC 69804-002-05), b) 2 OZ (NDC 69804-002-02), and c) 4 OZ (NDC 69804-002-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.
Reported: September 25, 2019 Initiated: August 9, 2019 #D-1856-2019
Product Description
PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4%, packaged in a) 1 OZ (NDC 69804-002-05), b) 2 OZ (NDC 69804-002-02), and c) 4 OZ (NDC 69804-002-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.
Reason for Recall
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Details
- Recalling Firm
- Ridge Properties, LLC
- Units Affected
- 383.65 ounces total
- Distribution
- Nationwide in the USA via internet sales through Amazon.com; ebay.com; Walmart.com; tatbalm.net; Naturallyhl.com
- Location
- Salem, OR
Frequently Asked Questions
What product was recalled? ▼
PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream, 4%, packaged in a) 1 OZ (NDC 69804-002-05), b) 2 OZ (NDC 69804-002-02), and c) 4 OZ (NDC 69804-002-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.. Recalled by Ridge Properties, LLC. Units affected: 383.65 ounces total.
Why was this product recalled? ▼
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 25, 2019. Severity: Moderate. Recall number: D-1856-2019.
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