TRP recalls sterile eye drops that may not be sterile due to lack of assurance of sterility. Consumers should check lot numbers and contact TRP for details.
Lack of Assurance of Sterility
TRP is recalling sterile eye drops that may not be sterile. This could lead to infections if used improperly. The recall affects specific lot numbers and expiration dates.
The eye drops lack assurance of sterility, meaning they might not be clean enough to use safely. This could cause infections if the drops are used without proper hygiene.
People who purchased TRP Natural Eyes Floaters Relief eye drops with lot numbers F404, F405, or F406 are affected. Those with the product are most at risk.
Check the lot number on the bottle, which is F404, F405, or F406. The product was sold with specific expiration dates: May 14, 2025, August 24, 2025, or October 11, 2026.
Look for lot numbers F404, F405, or F406 on the bottle.
The product lacks assurance of sterility, which could lead to infections if used.
Check the lot number on the bottle; it should be F404, F405, or F406.
Contact TRP for instructions on what to do with the product.
We’ve drafted a message you can send TRP to request your refund or repair — edit it as you like.
Subject: Recall D-0380-2024 — TRP TRP Hello, I own a TRP that is covered by recall D-0380-2024 from TRP. 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.
