Pharmacy Innovations recalls Acetylcysteine 10% Ophthalmic Solution due to FDA finding insanitary conditions at manufacturing facility. This may cause infections if used.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Acetylcysteine 10% Ophthalmic Solution (Rx only) because FDA inspections found unsanitary conditions at their Erie, PA facility. This could lead to eye infections if the product is used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility in Erie, PA. This lack of sterility could cause eye infections if the product is used. The product is for eye drops only and requires a prescription.
People who have the Acetylcysteine 10% Ophthalmic Solution (prescription-only) from Pharmacy Innovations. Those with eye conditions or recent eye surgery are at higher risk.
Check for the product name 'Acetylcysteine 10% Ophthalmic Solution' with prescription label. It was sold by Pharmacy Innovations at their Erie, PA location.
Look for the product name 'Acetylcysteine 10% Ophthalmic Solution' with prescription label.
The FDA found unsanitary conditions at the manufacturing facility, so the product may cause eye infections if used.
Check for the product name 'Acetylcysteine 10% Ophthalmic Solution' with prescription label from Pharmacy Innovations.
The recall does not specify a remedy, so contact Pharmacy Innovations for guidance.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0191-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0191-2023 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.