Assurance Infusion recalls BUP 4MG/FENT 3000MCG/ML 20mL syringes due to lack of sterility assurance. Affected lots: 12182019@7, expiring 12/27/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 4MG/FENT 3000MCG/ML 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly.
The syringes lack 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 the recalled syringes for medication injections. Those with medical conditions requiring frequent injections may be at higher risk.
Check for the lot number 12182019@7 on the syringe packaging. The syringes expire December 27, 2019.
Look for the lot number 12182019@7 on the syringe packaging.
BUP 4MG/FENT 3000MCG/ML 20mL syringes from Assurance Infusion with lot number 12182019@7.
Check for the lot number 12182019@7 on the syringe packaging. The syringes expire December 27, 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-0710-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0710-2020 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.
