Thrive Health Solutions recalls LX Bioboost Plus syringes due to lack of sterility assurance. This may cause infections if used. Consumers should check lot numbers and contact the company for details.
Lack of Assurance of Sterility
Thrive Health Solutions is recalling LX Bioboost Plus syringes because they lack sterility assurance. This could lead to infections if the product is used. Affected consumers should stop using the product and contact the company for instructions.
The product lacks sterility assurance, meaning it may not be clean enough to prevent infections. This could happen if the syringe is used for injections or other medical procedures.
People who purchased LX Bioboost Plus syringes from Thrive Health Solutions in Colorado. Those using the product for medical purposes are at higher risk.
Check the lot numbers: H227226 (exp 12/24/2025), H360175 (exp 6/2/2025), H368308 (exp 6/2/2025), or S360175 (exp 6/2/2025). The product is a pre-filled syringe containing specific vitamins and minerals.
Look for lot numbers H227226, H360175, H368308, or S360175 on the syringe label.
The product lacks sterility assurance, so it may cause infections if used. Do not use the product.
Check the lot numbers: H227226 (exp 12/24/2025), H360175 (exp 6/2/2025), H368308 (exp 6/2/2025), or S360175 (exp 6/2/2025).
The recall does not specify a remedy, so contact Thrive Health Solutions for instructions.
We’ve drafted a message you can send Thrive Health Solutions to request your refund or repair — edit it as you like.
Subject: Recall D-0477-2025 — Thrive Health Solutions Thrive Health Solutions Hello, I own a Thrive Health Solutions that is covered by recall D-0477-2025 from Thrive Health Solutions. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
