BioLyte Laboratories, LLC recalls NeoRelief for Muscle Cramping & Restlessness Homeopathic Topical Gel, packaged in a) 4 ml sample packs and b) Net Wt.
BioLyte recalls NeoRelief topical gel due to water contamination in some batches. Products with specific lot numbers and expiration dates are affected. Consumers should check labels for recalled lots.
Lower-risk recall
CGMP Deviations: finished product produced with active ingredients recalled by the manufacturer, King Bio Inc., due to water contamination issues that could potentially affect the quality of this product.
Contact the company & request your remedy
What happened, in plain English
BioLyte is recalling NeoRelief homeopathic topical gel for muscle cramping and restlessness due to water contamination in some batches. This could affect product quality but does not indicate a direct health risk. Read more at govinfonow.com/recall/39661-biolyte-neorelief-gel-recall-water-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39661-biolyte-neorelief-gel-recall-water-contamination-risk · Updated October 6, 2026 · FDA enforcement record: FDA #D-0002-2019
Cite this page
“BioLyte NeoRelief Gel Recall: Water Contamination Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39661-biolyte-neorelief-gel-recall-water-contamination-risk. Based on FDA recall #D-0002-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0002-2019%22&limit=1).
Why it’s dangerous
The gel was produced with water contamination issues that could affect product quality. This means the gel might not contain the intended active ingredients, but it does not indicate a direct health risk.
Who’s affected
Owners of NeoRelief gel in 4 ml sample packs or 2.0 oz bottles with specific lot numbers and expiration dates are affected. People using the product for muscle cramping or restlessness may be at risk if the gel has water contamination.
How to tell if you have this one
Check for 4 ml sample packs or 2.0 oz bottles with lot numbers 1146 (exp 3/29/20), 1138/1139 (exp 1/31/20), or 1160 (exp 10/10/19).
- Brand
BioLyte- Category
Drug
What to do — step by step
Check Product Label
Look for lot numbers and expiration dates on the gel container to determine if it is recalled.
Questions people ask
Is this product safe to use?
The recall is due to water contamination that could affect product quality, but it does not indicate a direct health risk.
What should I do if I have the recalled product?
The official recall notice does not specify a remedy, so check the product label for lot numbers and expiration dates to determine if it is recalled.
How can I tell if my NeoRelief gel is recalled?
Check for 4 ml sample packs or 2.0 oz bottles with lot numbers 1146 (exp 3/29/20), 1138/1139 (exp 1/31/20), or 1160 (exp 10/10/19).
Contact BioLyte
We’ve drafted a message you can send BioLyte to request your refund or repair — edit it as you like.
Subject: Recall D-0002-2019 — BioLyte BioLyte Hello, I own a BioLyte that is covered by recall D-0002-2019 from BioLyte. 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-0002-2019 (August 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0002-2019 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.