Assurance Infusion recalls BAC 15MCG/HYDROM 15MG/ML injection in 20mL syringes due to lack of sterility assurance. Affected lots: 12112019@23 expiring 12/20/2019.
Lack of sterility assurance.
Assurance Infusion is recalling a specific injection product because it lacks sterility assurance. This means the product could be contaminated and unsafe for use, potentially causing infections or other health issues.
The product lacks sterility assurance, meaning it may contain harmful bacteria or other contaminants. This could lead to infections or other health complications if used improperly.
People who own or use this injection product, particularly those with medical conditions requiring regular injections, are at risk of infection from contaminated medication.
Check for the lot number 12112019@23 on the syringe packaging. The product expires December 20, 2019.
Look for the lot number 12112019@23 on the syringe packaging.
The product lacks sterility assurance, so it is not safe to use. It may contain harmful contaminants that could cause infections.
The recall record does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for guidance.
Check for the lot number 12112019@23 on the syringe packaging. The product expires December 20, 2019.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0665-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0665-2020 from Assurance Infusion. 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.
