Assurance Infusion recalls BUP 2MG/ HYDROM 2MG/ML INJ in 20 mL syringes due to lack of sterility assurance. Affected lots expire 12/25/2019. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 2MG/ HYDROM 2MG/ML INJ in 20 mL syringes because they lack sterility assurance. This could lead to infections if used improperly. Consumers should check the lot number and contact the manufacturer for instructions.
The syringes lack sterility assurance, meaning they may not be clean enough to prevent infections when used. This could happen if the syringes are contaminated during manufacturing or handling.
People who have the BUP 2MG/ HYDROM 2MG/ML INJ in 20 mL syringes with lot number 12162019@10 are affected. Those using these syringes for medical purposes are at risk of infection.
Check the syringe label for the lot number 12162019@10. The expiration date is 12/25/2019. These syringes were sold by Assurance Infusion.
Look for the lot number 12162019@10 on the syringe label.
The lot number is 12162019@10.
The expiration date is 12/25/2019.
Call Assurance Infusion at (713) 533-8800.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0697-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0697-2020 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.
