AMMAN PHARMACEUTICAL INDUSTRIES recalls TRP Natural Eyes Sterile Eye Drops due to lack of assurance of sterility. Affected lots manufactured in Jordan with specific expiration dates. Consumers should check labels for lot numbers and expiration dates.
Lack of Assurance of Sterility
AMMAN PHARMACEUTICAL INDUSTRIES is recalling TRP Natural Eyes Sterile Eye Drops because they may not be sterile. This could lead to infections if used. The recall covers specific lots manufactured in Jordan with expiration dates.
The eye drops may not be sterile, which can cause infections in the eyes. This is a serious health risk, especially for individuals with weakened immune systems or existing eye conditions.
People who own or use TRP Natural Eyes Sterile Eye Drops with the specific lot numbers and expiration dates listed in the recall. Those with sensitive eyes or compromised immune systems are at higher risk.
Check the product label for the lot number and expiration date. The affected lots include FR001 (exp 07/24), FR004 (exp 04/25), FR005 (exp 04/25), FR006 (exp 04/25), and FR007 (exp 04/25).
Look for the lot number and expiration date on the product label to determine if it is affected.
The product may not be sterile, which can lead to eye infections.
Affected lots are FR001 (exp 07/24), FR004 (exp 04/25), FR005 (exp 04/25), FR006 (exp 04/25), and FR007 (exp 04/25).
Check the product label for the lot number and expiration date. If it matches the affected lots listed, it is part of the recall.
We’ve drafted a message you can send AMMAN PHARMACEUTICAL INDUSTRIES to request your refund or repair — edit it as you like.
Subject: Recall D-1156-2023 — AMMAN PHARMACEUTICAL INDUSTRIES AMMAN PHARMACEUTICAL INDUSTRIES Hello, I own a AMMAN PHARMACEUTICAL INDUSTRIES that is covered by recall D-1156-2023 from AMMAN PHARMACEUTICAL INDUSTRIES. 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.