ASP CARES recalls Biotin Solution for Injection (10 mg/mL, 30 mL vial) due to lack of sterility assurance. This product requires a prescription and is used for medical injections. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
ASP CARES is recalling Biotin Solution for Injection vials because they may not be sterile. This could lead to infections if used improperly. The product is prescription-only and requires careful handling.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. If injected, this could cause infections or other medical complications. The product is intended for medical use only and requires strict handling.
Prescription patients using this injectable biotin solution are affected. Healthcare providers who administer the product are at higher risk due to its medical use.
Check for the product name 'Biotin Solution for Injection', 10 mg/mL, 30 mL vial, with NDC 72833-0589-30. The lot number 091721589 and expiration date 03/16/2022 are also specific identifiers.
Reach out to ASP CARES at 2414 Babcock Rd Ste #106, San Antonio, TX 78229 for further instructions.
The recall indicates a lack of sterility assurance, so it is not safe for medical use. The product should not be used until the manufacturer provides instructions.
Look for the product name 'Biotin Solution for Injection', 10 mg/mL, 30 mL vial, with NDC 72833-0589-30 and lot number 091721589.
Contact ASP CARES at 2414 Babcock Rd Ste #106, San Antonio, TX 78229 for specific instructions on what to do with the product.
We’ve drafted a message you can send ASP CARES to request your refund or repair — edit it as you like.
Subject: Recall D-0261-2022 — ASP CARES ASP CARES Hello, I own a ASP CARES that is covered by recall D-0261-2022 from ASP CARES. 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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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.
