Vital Care Compounder recalls AutoLogus Tears Serum Soln Full Strength 3mL droptainers due to lack of sterility assurance from FDA inspection. Products may cause infection if used.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Vital Care Compounder is recalling AutoLogus Tears Serum Soln Full Strength 3mL droptainers because FDA found they were not produced with enough sterility assurance. Using these products could lead to infection if they are not sterile.
FDA inspections found the products were made without sufficient sterility assurance. This means the products might not be sterile, increasing the risk of infection if used for medical purposes.
People who have the recalled AutoLogus Tears Serum Soln Full Strength 3mL droptainers for medical use are affected. Those with compromised immune systems are at higher risk for infection.
Check for the product name 'AutoLogus Tears Serum Soln Full Strength 3mL droptainers' from Vital Care Compounder. Look for lot numbers 65521 through 66928 with specific expiration dates listed in the recall notice.
Look for the lot number on the droptainer label to see if it matches the recalled lots listed in the notice.
If you have the recalled product, talk to your doctor or pharmacist about potential risks and next steps.
FDA inspections found the products were produced without sufficient sterility assurance, which could lead to infection if used.
Check the lot number on the droptainer to see if it's in the recalled list. Then contact your healthcare provider for advice.
People with weakened immune systems are at higher risk for infection from non-sterile products.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0028-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0028-2023 from Vital Care Compounder. 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.
