Assurance Infusion recalls BUP 35MG/FENT 1.5MG/ML in 20 mL syringes due to lack of sterility assurance. Affected lots expire 12/20/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 35MG/FENT 1.5MG/ML in 20 mL syringes because they lack sterility assurance. This could lead to infections if used improperly.
The syringes lack sterility assurance, meaning they might not be clean enough to prevent infections. If used for injections, this could cause infections in the user.
People who own or use these syringes for medical injections are affected. Those with compromised immune systems may be at higher risk.
Check for the lot number 12112019@17 on the syringe. These syringes were sold with an expiration date of 12/20/2019.
Look for the lot number 12112019@17 on the syringe.
Assurance Infusion is recalling BUP 35MG/FENT 1.5MG/ML in 20 mL syringes due to lack of sterility assurance.
Check for the lot number 12112019@17 on the syringe. These syringes were sold with an expiration date of 12/20/2019.
The recall record does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for further instructions.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0703-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0703-2020 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.
