Assurance Infusion recalls morphine 5mg/ml injection in 20mL syringes due to lack of sterility assurance. Affected lots expire December 2019. Consumers should contact the manufacturer for details.
Lack of sterility assurance.
Assurance Infusion is recalling morphine 5mg/ml injection in 20mL syringes because they may not be sterile. This could lead to infections if used improperly.
The syringes lack sterility assurance, meaning they could be contaminated with bacteria. If used, this could cause infections or serious health issues.
People who have received the specific morphine syringes with lot numbers 12122019 or 12162019 are affected. Patients using this medication for pain management are at risk.
Check for lot numbers 12122019 or 12162019 on the syringe packaging. These syringes were sold with expiration dates of December 2019.
Call Assurance Infusion at (713) 533-8800 for specific recall details and instructions.
Assurance Infusion is recalling morphine 5mg/ml injection in 20mL syringes with lot numbers 12122019 or 12162019 due to lack of sterility assurance.
Look for lot numbers 12122019 or 12162019 on the syringe packaging. These syringes expire by December 2019.
Contact Assurance Infusion at (713) 533-8800 for specific instructions on what to do with the product.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0759-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0759-2020 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.
