Pine Pharmaceuticals recalls Tropi-Phen ophthalmic solution due to lack of sterility assurance. This compounded medication may cause infections if used improperly. Affected lots expire 10/16/2023 or 1/30/2024.
Lack of Assurance of Sterility
Pine Pharmaceuticals is recalling Tropi-Phen ophthalmic solution because it lacks sterility assurance. This means the medication could become contaminated and cause eye infections if used. The recall affects compounded products with specific lot numbers and expiration dates.
The medication lacks sterility assurance, meaning it could become contaminated with bacteria during production. This contamination risk could lead to eye infections if the solution is used without proper cleaning or sterilization.
People who have been prescribed this compounded eye drop medication are affected. Those with the specific lot numbers (67659 or 70316) and expiration dates (10/16/2023 or 1/30/2024) are most at risk.
Check the product label for the lot number: 67659 (expires 10/16/2023) or 70316 (expires 1/30/2024). This compounded eye drop is only available by prescription.
Look for lot numbers 67659 (expires 10/16/2023) or 70316 (expires 1/30/2024) on the packaging.
The recall indicates a lack of sterility assurance, so it may cause infections. Do not use this product without checking the recall status.
Check the product label for the lot numbers mentioned. If you have the affected lots, contact your doctor or pharmacist for guidance.
Look for lot numbers 67659 (expires 10/16/2023) or 70316 (expires 1/30/2024) on the packaging. This medication is only available by prescription.
We’ve drafted a message you can send Pine Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0063-2024 — Pine Pharmaceuticals Pine Pharmaceuticals Hello, I own a Pine Pharmaceuticals that is covered by recall D-0063-2024 from Pine Pharmaceuticals. 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.
