Assurance Infusion recalls BUP 30MG/MORP 8MG/ML in 20mL syringes due to lack of sterility assurance. Affected lots: 12122019@11 (expiring 12/21/2019).
Lack of sterility assurance.
Assurance Infusion is recalling a specific pain medication syringe because it may not be sterile. This could lead to infections if used improperly. The recall affects certain lots with a specific expiration date.
The syringe lacks sterility assurance, meaning it could be contaminated with bacteria. If used, this might cause infections or other health issues. The hazard is not described in detail about how it happens or the severity.
People who have the specific syringe lot 12122019@11 (expiring 12/21/2019) are affected. Healthcare providers and patients using this medication are at risk.
Check for the lot number 12122019@11 on the syringe. The syringe expires on December 21, 2019. This product was sold by Assurance Infusion.
Look for the lot number 12122019@11 on the syringe packaging.
The recall states there is a lack of sterility assurance, so it is not safe to use.
The recall does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for further instructions.
The product was sold with the lot number 12122019@11, expiring 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-0701-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0701-2020 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.
