Ridge Properties, LLC recalls 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
Ridge Properties LLC recalls PRE-TAT 4% lidocaine tattoo prep gel due to microbial contamination. Products may have unsafe lidocaine levels. Consumers should contact the manufacturer for details.
Recall notice
Microbial Contamination of Non-Sterile Products: products were found to be contaminated and above specification for lidocaine assay.
Contact the company & request your remedy
What happened, in plain English
Ridge Properties LLC is recalling PRE-TAT tattoo prep gel products that were found to have microbial contamination and unsafe lidocaine levels. Using these products could lead to health risks from the contamination. Read more at govinfonow.com/recall/38186-ridge-properties-pre-tat-tattoo-prep-gel-recall-microbial-contamination.
Source Summary by GovInfoNow · govinfonow.com/recall/38186-ridge-properties-pre-tat-tattoo-prep-gel-recall-microbial-contamination · Updated October 5, 2026 · FDA enforcement record: FDA #D-1857-2019
Cite this page
“Ridge Properties PRE-TAT Tattoo Prep Gel Recall: Microbial Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38186-ridge-properties-pre-tat-tattoo-prep-gel-recall-microbial-contamination. Based on FDA recall #D-1857-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1857-2019%22&limit=1).
Why it’s dangerous
The products were found to have microbial contamination and lidocaine levels above the specified safety standards. This could cause health issues if the product is used, especially for people with sensitive skin or those using it for tattooing.
Who’s affected
People who purchased PRE-TAT tattoo prep gel products from Ridge Properties LLC. Those with sensitive skin or who plan to use the product for tattooing are at higher risk.
How to tell if you have this one
Check for PRE-TAT 4% lidocaine tattoo prep gel bottles labeled with NDC codes 69804-019-14 (1 oz), 69804-019-15 (2 oz), or 69804-019-16 (4 oz). Products were sold online and in stores from Ridge Properties LLC in Salem, Oregon.
- Brand
Ridge Properties- Category
Drug
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Nationwide in the USA via internet sales through Amazon.com; ebay.com; Walmart.com; tatbalm.net; Naturallyhl.com
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1856-2019 | 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.; Lot # 1222, Exp 06/14/2023 | 383.65 ounces total |
| 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), and c) 4 Oz (NDC 69804-019-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.; Lot # 1213, Exp 06/05/2023 | 109.64 ounces total |
| D-1858-2019 | Superior Pain & Itch Relief (lidocaine) Cream, 4%, packaged in a) 1 OZ (NDC 69804-070-05), b) 2 OZ (NDC 69804-070-02), and c) 4 OZ (NDC 69804-070-03) jars, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.; Lot # 1222, Exp 06/14/2023 | 383.65 ounces total |
| D-1859-2019 | 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.; Lot # 1213, Exp 06/05/2023 | 109.64 ounces total |
| D-1860-2019 | 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.; Lot # 1228, Exp 06/21/2023 | 136 ounces |
| D-1861-2019 | Soothing Sore Relief (lidocaine) Liquid Gel, 4%, packaged in a) 1 Oz (NDC 69804-077-14), b) 2 Oz (NDC 69804-077-15), and c) 4 Oz (NDC 69804-077-16) bottles, OTC, Manufactured, packed & distributed by Pain Relief Naturally, Salem, OR 97301.; Lot # 1135, Exp 12/27/2022 | 104.1 ounces |
What to do — step by step
Check Product Labels
Look for NDC codes 69804-019-14, 69804-019-15, or 69804-019-16 on the product packaging.
Questions people ask
Is this product safe to use?
The recall states the products were found to have microbial contamination and unsafe lidocaine levels, so they are not safe to use.
How can I get a refund or replacement?
The recall record does not mention any remedy or refund process.
What should I do if I have this product?
The recall record does not specify any action steps beyond checking the product labels.
Contact Ridge Properties
We’ve drafted a message you can send Ridge Properties to request your refund or repair — edit it as you like.
Subject: Recall D-1857-2019 — Ridge Properties Ridge Properties Hello, I own a Ridge Properties that is covered by recall D-1857-2019 from Ridge Properties. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1857-2019 (August 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1857-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.