Assurance Infusion recalls 20mL syringes with lot 12172019@3 exp 12/26/2019 due to lack of sterility assurance. Consumers should contact the manufacturer for details.
Lack of sterility assurance.
Assurance Infusion is recalling a specific type of 20mL syringe because it may not be sterile. This could lead to infections if used for medical purposes.
The syringes lack sterility assurance, meaning they might not be clean enough to prevent infections. This is a risk during medical procedures where sterile equipment is critical.
Patients using this syringe for medical treatments are affected. Healthcare providers handling these syringes may also be at risk.
Check for the lot number 12172019@3 and expiration date 12/26/2019 on the syringe packaging. The product is manufactured by Assurance Infusion.
Reach out to Assurance Infusion at (713) 533-8800 for specific recall details and instructions.
The recall indicates a lack of sterility assurance, so it is not safe for medical use.
Contact Assurance Infusion at (713) 533-8800 for guidance on next steps.
Look for the lot number 12172019@3 and expiration date 12/26/2019 on the syringe packaging.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0668-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0668-2020 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.
