TRP recalls sterile eye ointment due to lack of sterility assurance. Products manufactured in Jordan with specific lots may cause infection. Stop using and contact TRP for details.
Lack of Assurance of Sterility
TRP is recalling sterile eye ointment products that may not be sterile, which could lead to eye infections. This recall affects specific lots manufactured in Jordan and sold in the U.S. from 2023 to 2024.
The ointment may not be sterile, which could lead to infections in the eye. This risk is especially concerning for individuals with open wounds or weakened immune systems.
People who own or use TRP Natural Eyes, Stye Relief, or Sterile Eye Ointment products with the listed lots. Those with sensitive eyes or compromised immune systems are at higher risk.
Check the product label for the lot numbers listed: 182002 through 182011, with expiration dates up to March 2025. Products were manufactured in Jordan and sold exclusively by TRP Company, Inc. in Reno, Nevada.
Look for lot numbers 182002 through 182011 on the product label.
The recall states there is a lack of assurance of sterility, so it may not be safe. Do not use these products.
The recall record does not mention a replacement or remedy.
The recall record does not specify a remedy, so contact TRP Company, Inc. for guidance.
We’ve drafted a message you can send TRP to request your refund or repair — edit it as you like.
Subject: Recall D-1165-2023 — TRP TRP Hello, I own a TRP that is covered by recall D-1165-2023 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.
