Assurance Infusion recalls BUP 15MG/CLON 300MCG/FENT 1500MCG/ML(40) 20mL syringes due to lack of sterility assurance. Affected units have lot number 12122019@6 expiring 12/21/2019.
Lack of sterility assurance.
Assurance Infusion is recalling a specific type of 20mL syringe that contains BUP 15MG/CLON 300MCG/FENT 1500MCG. The recall is due to a lack of sterility assurance, which could lead to infections if used.
The syringes lack sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used for injections, this could cause infections in the user.
Patients using this specific syringe for medical injections are affected. Those with the lot number 12122019@6 (expiring 12/21/2019) are most at risk.
Check for the lot number 12122019@6 on the syringe packaging. The syringe contains BUP 15MG/CLON 300MCG/FENT 1500MCG in a 20mL size.
Look for the lot number 12122019@6 on the syringe packaging.
BUP 15MG/CLON 300MCG/FENT 1500MCG in a 20mL syringe from Assurance Infusion.
Lot number 12122019@6 (expiring 12/21/2019).
The recall record does not specify a remedy.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0683-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0683-2020 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.
