TRP recalls sterile eye drops due to lack of assurance of sterility. Products manufactured in Jordan with specific lot numbers and expiration dates are affected. Consumers should contact TRP for details.
Lack of Assurance of Sterility
TRP is recalling sterile eye drops that may not be sterile, which can cause infections. This recall affects products made in Jordan with specific lot numbers and expiration dates.
The eye drops lack assurance of sterility, meaning they could contain harmful bacteria or other contaminants. If used, this could lead to eye infections, especially in individuals with weakened immune systems or existing eye conditions.
People who own or use TRP Natural Eyes, Floaters Relief, or Sterile Eye drops with the specified lot numbers and expiration dates are affected. Those with compromised immune systems or existing eye conditions may be at higher risk.
Check the product label for the lot numbers DA001 (expiring June 2024) and DA002 (expiring November 2024). The products were manufactured in Jordan and sold by TRP Company, Inc. in Reno, Nevada.
Look for lot numbers DA001 (expiring June 2024) or DA002 (expiring November 2024) on the eye drop container.
The recall states there is a lack of assurance of sterility, so they may not be safe. Do not use these products until you confirm they are not affected.
Check the product label for the lot numbers DA001 or DA002. If you have these lot numbers, contact TRP Company, Inc. for instructions.
The recall record does not mention a replacement option. Contact TRP Company, Inc. directly for details on what to do with the affected products.
We’ve drafted a message you can send TRP to request your refund or repair — edit it as you like.
Subject: Recall D-1159-2023 — TRP TRP Hello, I own a TRP that is covered by recall D-1159-2023 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.
