Assurance Infusion recalls BUP 5MG/MORP 20MG/ML 20mL syringes due to lack of sterility assurance. Affected lots: 12162019@6, expiring 12/25/2019.
Lack of sterility assurance.
Assurance Infusion is recalling BUP 5MG/MORP 20MG/ML 20mL syringes because they lack sterility assurance. This could lead to infections if used improperly.
The syringes lack sterility assurance, meaning they may not be clean enough to prevent infections when used for medical injections. This poses a risk of contamination and potential infection in patients.
People who have the specific lot numbers (12162019@6) of this syringe product are affected. Healthcare providers using these syringes for medical injections are at higher risk.
Check for the lot number 12162019@6 on the syringe packaging. The syringes expire on December 25, 2019.
Look for the lot number 12162019@6 on the syringe packaging.
The affected lot number is 12162019@6.
The syringes expire on December 25, 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-0715-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0715-2020 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.
