Assurance Infusion recalls 20mL syringes with potential lack of sterility. Affected lots may pose infection risks. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling 20mL syringes that may not be sterile, which could lead to infections if used. This is a serious safety issue requiring immediate attention.
The syringes lack sterility assurance, meaning they could be contaminated with bacteria or other pathogens. If used for injections, this could cause infections in patients.
Patients using the recalled syringes for medical treatments are at risk of infection. Healthcare providers administering these syringes should also check their inventory.
Check for the lot number 12172019@2 with expiration date 12/26/2019 on the syringe. The product is labeled as BAC 150 mcg/BUP 2 mg/Hydrom 15 mg/Morp 20 mg/SUF 650 mcg/mL in 20 mL syringe.
Immediately discard any syringes with lot number 12172019@2 that expired by December 26, 2019.
No, the recalled syringes lack sterility assurance and could cause infections if used.
Look for the lot number 12172019@2 with expiration date 12/26/2019 on the syringe label.
Immediately discard them and contact Assurance Infusion at (713)533-8800 for further instructions.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0664-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0664-2020 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.
