Assurance Infusion recalls morphine 18mg/ml injection in 20mL syringes due to lack of sterility assurance. Affected lots expired 12/25/2019. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling morphine 18mg/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 in patients. The hazard is not described as causing serious injury in normal use.
People who received this morphine injection in 20mL syringes from Assurance Infusion. Patients using this specific product are at risk of infection.
Check for the product name 'Morphine 18mg/ml INJ in 20 mL syringe' from Assurance Infusion. The lot number starts with 12162019 and expires 12/25/2019.
Call Assurance Infusion at (713) 533-8800 for details about the recall and next steps.
The recall states there is a lack of sterility assurance, so it is not safe to use. Contact Assurance Infusion for details.
Contact Assurance Infusion at (713) 533-8800 for instructions on what to do with the product.
Look for the product name 'Morphine 18mg/ml INJ in 20 mL syringe' with lot number starting with 12162019 and expiration date 12/25/2019.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0753-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0753-2020 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.
