Assurance Infusion recalls BUP 40MG/MORP 4MG/ML in 20mL syringes due to lack of sterility assurance. Affected lots: 12172019@4, expiring 12/26/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 40MG/MORP 4MG/ML injections in 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly. The recall affects specific lots with an expiration date of December 26, 2019.
The syringes lack sterility assurance, meaning they may not be clean enough to prevent infections when used for injections. This could lead to serious infections if the medication is administered through an unsterile syringe.
Patients using the recalled syringes for medication injections. Those with the specific lot number 12172019@4 and expiration date 12/26/2019 are most at risk.
Check for the lot number 12172019@4 on the syringe packaging. The syringe expires on December 26, 2019. The product is labeled as BUP 40MG/MORP 4MG/ML in 20mL syringe.
Look for the lot number 12172019@4 and expiration date of December 26, 2019 on the syringe packaging.
The specific lot number is 12172019@4.
This syringe expires on December 26, 2019.
The recall record does not specify a remedy.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0709-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0709-2020 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.
