Assurance Infusion recalls BUP 30mg/Fent 400mcg/mL 20mL syringes due to lack of sterility assurance. Affected lots: 12132019@3, expiring 12/22/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 30mg/Fent 400mcg/mL 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly.
The syringes lack proper sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used for injections, this could cause infections or other health issues.
Patients using this specific syringe for medication injections are affected. Those with the lot number 12132019@3 and expiration date 12/22/2019 are most at risk.
Check for the lot number 12132019@3 on the syringe packaging. The expiration date is 12/22/2019. This product was sold by Assurance Infusion.
Look for the lot number 12132019@3 and expiration date 12/22/2019 on the syringe packaging.
The recall states there is a lack of sterility assurance, so it is not safe to use. The product should be discarded or returned.
The recall does not specify a remedy, so you should contact Assurance Infusion at (713) 533-8800 for further instructions.
Check for the lot number 12132019@3 and expiration date 12/22/2019 on the syringe packaging.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0699-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0699-2020 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.
