RXQ Compounding recalls NIACINAMIDE 100mg/ml vials due to lack of sterility assurance. All lots within expiry date are affected. Consumers should contact the company for guidance.
Lack of Assurance of Sterility
RXQ Compounding is recalling NIACINAMIDE 100mg/ml vials because they may not be sterile. This could lead to infections if used improperly. The recall covers all vials produced within the expiry date.
The product may not be sterile, which can lead to infections if the solution is used for medical purposes. This lack of sterility assurance could cause serious health issues if the vial is not properly handled.
People who have purchased NIACINAMIDE 100mg/ml vials from RXQ Compounding in the US. Those using the product for medical purposes are at higher risk due to potential contamination.
Check for the product name 'NIACINAMIDE 100MG/ML, 10ML per vial' and the manufacturer 'RXQ Compounding LLC'. The recall covers all vials produced within the expiry date.
Reach out to RXQ Compounding LLC at 340 West State Street, Unit 9, Athens, OH 45701 for specific guidance on the recalled product.
The recall indicates a lack of sterility assurance, so the product may not be safe for medical use. Contact the manufacturer for specific guidance.
Look for the product name 'NIACINAMIDE 100MG/ML, 10ML per vial' and the manufacturer 'RXQ Compounding LLC'. The recall covers all vials within the expiry date.
Contact RXQ Compounding LLC at 340 West State Street, Unit 9, Athens, OH 45701 for specific instructions on handling the recalled product.
We’ve drafted a message you can send RXQ Compounding to request your refund or repair — edit it as you like.
Subject: Recall D-1689-2019 — RXQ Compounding RXQ Compounding Hello, I own a RXQ Compounding that is covered by recall D-1689-2019 from RXQ Compounding. 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.
