Delsam Pharma's Artificial Eye Ointment (3.5g tube) recalled due to bacterial contamination in unopened tubes. FDA analysis found unsterile product. Consumers should stop using affected batches.
Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.
Delsam Pharma is recalling artificial eye ointment tubes that were found contaminated with bacteria by FDA analysis. Using unopened tubes could lead to infection or other health risks.
FDA analysis found bacterial contamination in unopened tubes. Bacteria can cause eye infections, which may lead to serious complications if not treated properly.
People who own or use the recalled artificial eye ointment tubes. Those with eye conditions or recent eye surgery are at higher risk.
Check for the 3.5 grams (1/8 oz.) tube labeled with NDC 72570 122 35, batch number H29, and expiration date 11/30/2023. The product was distributed by Delsam Pharma in New York.
Immediately stop using any unopened tubes of the recalled artificial eye ointment as they contain bacteria that can cause infection.
No, FDA analysis found bacterial contamination in unopened tubes, making them unsafe for use.
Check for the 3.5 grams (1/8 oz.) tube with NDC 72570 122 35, batch number H29, and expiration date 11/30/2023.
Immediately stop using it and dispose of the tube safely.
We’ve drafted a message you can send Delsam Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0488-2023 — Delsam Pharma Delsam Pharma Hello, I own a Delsam Pharma that is covered by recall D-0488-2023 from Delsam Pharma. 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.
