Assurance Infusion recalls 20mL syringes with BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG due to lack of sterility assurance. Affected lots: 12102019@3 expiring 12/19/2019.
Lack of sterility assurance.
Assurance Infusion is recalling a specific 20mL syringe containing certain medications because it lacks sterility assurance. This could lead to infections if used improperly. The recall affects syringes with lot number 12102019@3 that expire December 19, 2019.
The syringe lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. If used for injections, this could cause infections in patients. The lack of sterility is a critical issue for medical devices that come into direct contact with the body.
People who have the specific syringe with lot number 12102019@3 expiring December 19, 2019 are affected. Healthcare providers using this syringe for medication administration are most at risk.
Check for the lot number 12102019@3 on the syringe packaging. The syringe contains BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG in 20 mL. It expires December 19, 2019.
Look for the lot number 12102019@3 on the syringe packaging.
The specific product is a 20mL syringe containing BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG that was manufactured with lot number 12102019@3 and expires December 19, 2019.
Check for the lot number 12102019@3 on the syringe packaging. The syringe contains BUP 2.5MG/FENT 25MCG/HYDRO 2MG/MORP 40MG in 20 mL and expires December 19, 2019.
The recall record does not specify a remedy, so the official notice does not provide instructions on what to do with the recalled syringe.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0690-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0690-2020 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.
