TRP recalls sterile eye drops due to lack of sterility assurance. Products manufactured for TRP Company, Inc. with specific lot numbers and expiration dates are affected. Consumers should check labels and contact TRP for details.
Lack of Assurance of Sterility
TRP is recalling sterile eye drops that may not be sterile, which could lead to infections. This recall affects specific lot numbers and expiration dates of the product.
The eye drops lack assurance of sterility, meaning they might not be clean enough to prevent infections. Using non-sterile eye drops can lead to serious eye infections or other health issues.
People who own or use the TRP Natural Eyes Dryness Relief eye drops with the specific lot numbers and expiration dates listed in the recall are affected. Those with the product are at risk of infection if the drops are not sterile.
Check the product label for the lot numbers D101, D102, or D103 and expiration dates listed in the recall. The product is sold in 0.33 fl oz (10 mL) containers.
Look for lot numbers D101, D102, or D103 and expiration dates on the container.
TRP Natural Eyes Dryness Relief Sterile Eye Drops, 0.33 fl oz (10 mL), manufactured for TRP Company, Inc. with lot numbers D101, D102, or D103.
Check the label for lot numbers D101, D102, or D103 and expiration dates listed in the recall.
The recall does not specify a remedy, so contact TRP directly for further instructions.
We’ve drafted a message you can send TRP to request your refund or repair — edit it as you like.
Subject: Recall D-0378-2024 — TRP TRP Hello, I own a TRP that is covered by recall D-0378-2024 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.
