AMMAN PHARMACEUTICAL INDUSTRIES recalls TRP Natural Eyes and Blur Relief Sterile Eye Drops (0.5 fl oz) manufactured in Jordan due to lack of sterility assurance. This could pose infection risks if used.
Lack of Assurance of Sterility
AMMAN PHARMACE: TRP Natural Eyes and Blur Relief Sterile Eye Drops (0.5 fl oz) are recalled because they may not be sterile. Using these products could lead to eye infections.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or other contaminants. This increases the risk of eye infections, especially if the product is used without proper hygiene.
People who own or use TRP Natural Eyes or Blur Relief Sterile Eye Drops manufactured in Jordan (lot DC001, expiring June 2024) are affected. Those with sensitive eyes or medical conditions may be at higher risk.
Check for the product name 'TRP Natural Eyes' or 'Blur Relief' Sterile Eye Drops, 0.5 fl oz (15 mL), manufactured in Jordan. The lot number is DC001 with an expiration date of June 2024.
Look for the product name, size (0.5 fl oz), and lot number DC001 on the packaging.
The recall states there is a lack of assurance of sterility, so it is not safe to use. The product may contain harmful contaminants.
Check for the product name 'TRP Natural Eyes' or 'Blur Relief' Sterile Eye Drops, 0.5 fl oz (15 mL), manufactured in Jordan with lot number DC001 and expiration date June 2024.
The recall does not specify a remedy, so contact the manufacturer for guidance on safe disposal or alternatives.
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-1154-2023 — AMMAN PHARMACEUTICAL INDUSTRIES AMMAN PHARMACEUTICAL INDUSTRIES Hello, I own a AMMAN PHARMACEUTICAL INDUSTRIES that is covered by recall D-1154-2023 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.
