Assurance Infusion recalls CLON 100MCG/MORP 12MG/ML injections in 20mL syringes due to lack of sterility assurance. This could lead to infections if used.
Lack of sterility assurance.
Assurance Infusion is recalling a specific injection product because it lacks sterility assurance. Using this product could lead to infections if it's not properly sterilized.
The product lacks sterility assurance, meaning it may not be clean enough to prevent infections. This could happen if the product is used without proper sterilization.
People who have the specific injection product with lot number 12122019 (expiring December 21, 2019) are affected. Healthcare providers and patients using this product are at risk.
Check for the product name 'CLON 100MCG/MORP 12MG/ML INJ in 20 mL syringe' from Assurance Infusion. The lot number is 12122019 and it expires December 21, 2019.
Look for the lot number 12122019 on the syringe packaging.
The product lacks sterility assurance, so it may not be safe to use and could lead to infections.
The recall record does not specify a remedy, so contact Assurance Infusion at (713) 533-8800 for guidance.
Check for the lot number 12122019 on the syringe packaging, which expires December 21, 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-0721-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0721-2020 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.
