Pharmacy Innovations recalls eye drops containing flurbiprofen-corn oil solution due to FDA findings of insanitary conditions at the manufacturing facility.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled a prescription eye drop product (flurbiprofen-corn oil 0.04% solution) because FDA inspections found unsanitary conditions at the facility. This could lead to contamination risks for users.
FDA inspections found unsanitary conditions at the manufacturing facility, which could lead to contamination of the product. This poses a risk of infection or other health issues for users.
Prescription eye drop users who purchased this specific product from Pharmacy Innovations. Those with eye conditions requiring this medication are at higher risk.
Check for the product name: FLURBIPROFEN -CORN OIL- 0.04% (3ML DROPTAINER) OPH SOLUTION. It was sold by Pharmacy Innovations in Erie, PA.
Look for the product name and manufacturer on the label to confirm if it matches the recalled item.
The FDA found unsanitary conditions at the facility, so the product may be contaminated. Do not use it.
The recall record does not mention a replacement or remedy.
Pharmacy Innovations in Erie, PA.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0208-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0208-2023 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.
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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.
