Assurance Infusion recalls BUP 5MG/MORP 10MG/ML in 20mL syringes due to lack of sterility assurance. Affected lots: 12122019@21 expiring 12/21/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 5MG/MORP 10MG/ML in 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly.
The syringes do not have adequate sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used for injections, this could cause infections or other health complications.
People using these syringes for medical injections, particularly those with compromised immune systems or chronic conditions.
Check for the lot number 12122019@21 on the syringe packaging. The syringes expire December 21, 2019.
Look for the lot number 12122019@21 on the syringe packaging.
The syringes lack sterility assurance, which could lead to infections if used for injections.
The recall record does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for further instructions.
Check for the lot number 12122019@21 on the syringe packaging. The syringes expire December 21, 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-0714-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0714-2020 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.
