Pharmacy Innovations recalls MITOMYCIN 0.2MG/ML Oph Solution products due to FDA finding insanitary conditions at manufacturing facility. Products may not be sterile, posing infection risks.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling two types of MITOMYCIN 0.2MG/ML ophthalmic solutions because an FDA inspection found unsanitary conditions at their facility. This means the products might not be sterile, which could lead to eye infections if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of sterility could mean the medication isn't safe for eye use, potentially causing infections.
People who have prescription MITOMYCIN 0.2MG/ML ophthalmic solutions from Pharmacy Innovations. Those with eye conditions requiring this medication are most at risk.
Check for the product names: MITOMYCIN 0.2MG/ML (1ML DROPTAINER) OPH SOLUTION or MITOMYCIN 0.2MG/ML (1ML VIAL) OPH SOLUTION. These are prescription-only products sold by Pharmacy Innovations.
Look for the product names and manufacturer on the packaging to confirm if it's part of this recall.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could mean the medication isn't sterile.
Check for the product names: MITOMYCIN 0.2MG/ML (1ML DROPTAINER) OPH SOLUTION or MITOMYCIN 0.2MG/ML (1ML VIAL) OPH SOLUTION, which are prescription-only products from Pharmacy Innovations.
The recall record does not specify a remedy, so contact Pharmacy Innovations directly 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-0223-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0223-2023 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.
