ANHUI WELCOME FOREIGN TRADE CO.,LTD. recalls Pi Yen Chin Ophthalmic Redness Reliever Drops (10ml) sold in the U.S. due to being manufactured as nasal drops but labeled as eye drops, risking infection.
Labeling: Not Elsewhere Classified; The packaging states these are ophthalmic drops. However, they are manufactured as nasal drops and sterility cannot be assured.
ANHUI WELCOME FOREIGN TRADE CO.,LTD. recalled Pi Yen Chin Ophthalmic Redness Reliever Drops sold in the U.S. because they are actually nasal drops, not eye drops, and may not be sterile. Using them in the eyes could cause infection.
The product is labeled as eye drops but is manufactured as nasal drops. Since it's not sterile, using it in the eyes could lead to infection or irritation.
People who bought Pi Yen Chin Ophthalmic Redness Reliever Drops (10ml) from U.S. distributors. Those using the product for eye relief are at risk of infection.
Check for the product name 'Pi Yen Chin Ophthalmic Redness Reliever Drops' with a 10ml size. Look for the distributor label from International Nature Nutraceuticals, Inc. in New York.
Look for the product name and size on the label to confirm it's the recalled version.
The product is labeled as eye drops but is manufactured as nasal drops, so it may not be sterile and could cause infection if used in the eyes.
Check for the product name 'Pi Yen Chin Ophthalmic Redness Reliever Drops' with a 10ml size and the distributor label from International Nature Nutraceuticals, Inc. in New York.
The recall does not specify a remedy, so contact the manufacturer or distributor for guidance.
We’ve drafted a message you can send ANHUI WELCOME FOREIGN TRADE CO.,LTD. to request your refund or repair — edit it as you like.
Subject: Recall D-0755-2021 — ANHUI WELCOME FOREIGN TRADE CO.,LTD. ANHUI WELCOME FOREIGN TRADE CO.,LTD. Hello, I own a ANHUI WELCOME FOREIGN TRADE CO.,LTD. that is covered by recall D-0755-2021 from ANHUI WELCOME FOREIGN TRADE CO.,LTD.. 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.
