Assurance Infusion recalls BUP 15MG/CLON 600MCG/MORP 30MG/ML (40) in 20mL syringes due to lack of sterility assurance. This may cause infections if used.
Lack of sterility assurance.
Assurance Infusion is recalling a specific pain medication syringe because it lacks sterility assurance. Using this syringe could lead to infections if the medication is injected.
The syringe lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. If used for injections, this could lead to infections or other health issues.
People who have the specific BUP 15MG/CLON 600MCG/MORP 30MG/ML (40) in 20mL syringe from Assurance Infusion. Those with medical conditions requiring injections are most at risk.
Check for the syringe labeled BUP 15MG/CLON 600MCG/MORP 30MG/ML (40) in 20mL. The lot number 12182019@2 with an expiration date of 12/27/2019.
Look for the syringe labeled BUP 15MG/CLON 600MCG/MORP 30MG/ML (40) in 20mL with lot number 12182019@2 and expiration date 12/27/2019.
No, this syringe lacks sterility assurance and could cause infections if used for injections.
Check the syringe details to confirm it's the recalled version. If it is, contact Assurance Infusion at (713) 533-8800 for instructions.
Look for the syringe labeled BUP 15MG/CLON 600MCG/MORP 30MG/ML (40) in 20mL with lot number 12182019@2 and expiration date 12/27/2019.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0685-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0685-2020 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.
