Assurance Infusion recalls morphine 2mg/ml injection in 20mL syringes due to lack of sterility assurance. Affected lots expire 12/25/2019. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling morphine 2mg/ml injection in 20mL syringes because they may not be sterile. This could lead to infections if used improperly.
The syringes may not be sterile, which could cause infections if the medication is injected. This is a risk during medical procedures where contamination might occur.
Patients using morphine injections in the U.S. who received this specific syringe model are affected. Healthcare providers administering the medication are at higher risk.
Check for the syringe model labeled 'MORPHINE 2MG/ML INJ in 20 mL syringe' from Assurance Infusion. The lot number starts with 12162019 and expires 12/25/2019.
Look for the lot number starting with 12162019 and expiration date 12/25/2019 on the syringe.
The recall states there is a lack of sterility assurance, so it is not safe to use. Contact Assurance Infusion for details.
Check for the syringe model labeled 'MORPHINE 2MG/ML INJ in 20 mL syringe' with lot number starting 12162019 and expiration 12/25/2019.
The recall does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for guidance.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0756-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0756-2020 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.