Assurance Infusion recalls BUP 1mg/mL Hydrom 7mg 20mL syringes due to lack of sterility assurance. Affected lots: 12112019@10, expiring 12/20/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 1mg/mL Hydrom 7mg 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly. Consumers should check their lot numbers and contact the manufacturer if they have the affected product.
The syringes lack sterility assurance, meaning they may not be clean enough to prevent infections when used. This could lead to serious infections if the syringe is used for injections without proper sterilization.
People who have the specific lot number 12112019@10 of Assurance Infusion BUP 1mg/mL Hydrom 7mg 20mL syringes. Healthcare professionals and patients using these syringes are most at risk.
Check for the lot number 12112019@10 on the syringe packaging. The syringes expire December 20, 2019, so they were sold between late 2018 and early 2019.
Look for the lot number 12112019@10 on the syringe packaging.
The lot number is 12112019@10.
The syringes expire December 20, 2019.
Contact Assurance Infusion at (713) 533-8800 to confirm if your syringes are affected.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0688-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0688-2020 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.
