Assurance Infusion recalls BUP 20MG/SUF 1000MCG/ML 20mL syringes due to lack of sterility assurance. This could lead to infections if used improperly.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 20MG/SUF 1000MCG/ML 20mL syringes because they lack sterility assurance. Using these syringes could lead to infections if they are not properly sterilized.
The syringes lack sterility assurance, meaning they may not be clean enough to prevent infections when used for medical injections. This could lead to serious infections if the syringes are not properly sterilized before use.
People who have the BUP 20MG/SUF 1000MCG/ML 20mL syringes with lot number 12172019@10 and expiration date 12/26/2019 are affected. Those using these syringes for medical purposes are at risk of infection.
Check for the lot number 12172019@10 and expiration date 12/26/2019 on the syringe packaging. The product is a BUP 20MG/SUF 1000MCG/ML 20mL syringe from Assurance Infusion.
Look for the lot number 12172019@10 and expiration date 12/26/2019 on the syringe packaging.
BUP 20MG/SUF 1000MCG/ML 20mL syringes from Assurance Infusion with lot number 12172019@10 and expiration date 12/26/2019.
The syringes lack sterility assurance, which could lead to infections if used improperly.
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-0693-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0693-2020 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.
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.