Pharmacy Innovations recalls TOBRAMYCIN FORTIFIED 15MG/ML OPH SOLUTION due to FDA finding insanitary conditions at manufacturing facility. This eye drop product is for prescription use only.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling prescription eye drops containing tobramycin fortified at 15mg/ml because FDA inspections found unsanitary conditions at their Erie, PA facility. This could lead to infections if the product is used without proper sterility.
FDA inspections found unsanitary conditions at the manufacturing facility. This lack of sterility could allow harmful bacteria to contaminate the product, potentially causing eye infections if used.
Prescription eye drop users who purchased this specific product from Pharmacy Innovations. People with eye conditions requiring this medication are at higher risk.
This product is labeled 'TOBRAMYCIN FORTIFIED 15MG/ML OPH SOLUTION, Rx Only' and was sold by Pharmacy Innovations in Erie, PA. The recall was issued on November 4, 2022.
Look for the product name and manufacturer details on the label to confirm if it matches the recalled item.
The FDA found unsanitary conditions at the manufacturing facility, so the product may not be sterile and could cause infections. Do not use it.
The recall record does not mention a replacement or remedy for this product.
This recall was issued on November 4, 2022.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0240-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0240-2023 from Pharmacy Innovations. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
