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Drug recall · FDA · Published October 3, 2018

Silver Star Brands recalls Native Remedies VaricoGo Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906.

Native Remedies VaricoGo Oral Spray (2 fl oz) recalled due to microbial contamination. Consumers should contact Silver Star Brands for details.

🇺🇸 FDA recall #D-0253-2019DrugNative Remedies ›
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Contact the company & request your remedy

Recalling firmSilver Star Brands2155 S Oakwood Rd · Oshkosh, WI 54904-6359
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Native Remedies is recalling its VaricoGo Oral Spray (2 fl oz bottles) because they may contain harmful bacteria. This poses a risk of infection if used. Read more at govinfonow.com/recall/39537-native-remedies-varicogo-oral-spray-recall-microbial-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/39537-native-remedies-varicogo-oral-spray-recall-microbial-contamination-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-0253-2019

Cite this page

“Native Remedies VaricoGo Oral Spray Recall: Microbial Contamination Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39537-native-remedies-varicogo-oral-spray-recall-microbial-contamination-risk. Based on FDA recall #D-0253-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0253-2019%22&limit=1).

Why it’s dangerous

The product may have been contaminated with bacteria during manufacturing. This can lead to infections if the spray is used orally, especially in people with weakened immune systems.

Who’s affected

People who own or use Native Remedies VaricoGo Oral Spray (2 fl oz) bottles with NDC 68703-105-59 and lot K111717A are affected. Those with compromised immune systems may be at higher risk.

How to tell if you have this one

Check for the product name 'VaricoGo Oral Spray', 2 fl oz (59 mL) per bottle, and the lot number K111717A on the label. The NDC code 68703-105-59 is also associated with this batch.

  • Brand
    Native Remedies
  • Category
    Drug
FDA recall event · 6 products

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.

  • Status
    Terminated
  • Distribution
    Nationwide USA
Recall numberProduct, codes & lotsQuantityClass
D-0251-2019Native Remedies VertiFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-253-02; Lot K061417B67 bottlesClass I
D-0252-2019Native Remedies HypoSlim Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-275-02; Lot K051818A95 bottlesClass I
D-0253-2019Native Remedies VaricoGo Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-105-59; Lot K111717A53 bottlesClass I
D-0254-2019Native Remedies EyeClear Pro Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-151-59; Lot K022317A and K022317B931 bottlesClass I
D-0255-2019Healthful Naturals DizziFree Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906. NDC 68703-204-02; Lot K022616D247 bottlesClass II
D-0256-2019Healthful Naturals Leg Cramp Support Oral Spray, 2 fl oz (59 mL) per bottle, Distributed by: Silver Star Brands, Oshkosh, WI 54906 NDC 68703-206-02; Lot K022216C247 bottlesClass II
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number K111717A and NDC 68703-105-59 on the label to confirm if your product is recalled.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a possible microbial contamination risk, so it is not recommended to use the product until the manufacturer provides further instructions.

How can I get a replacement?

The recall record does not specify a replacement process or contact information for replacements.

What should I do if I have this product?

The recall record does not state a specific action for affected consumers beyond checking product details.

Take action

Contact Native Remedies

We’ve drafted a message you can send Native Remedies to request your refund or repair — edit it as you like.

Subject: Recall D-0253-2019 — Native Remedies Native Remedies

Hello,

I own a Native Remedies that is covered by recall D-0253-2019 from Native Remedies.

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-0253-2019 (October 3, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0253-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA