Pharmacy Innovations recalls Estradiol 0.05% OPH Solution (Rx Only) due to FDA finding insanitary conditions at manufacturing facility. This may pose a risk of contamination.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innov: Estradiol 0.05% OPH Solution (prescription-only) has been recalled because an FDA inspection found unsanitary conditions at the manufacturing facility. This could lead to contamination risks for users.
The FDA 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 users of Estradiol 0.05% OPH Solution who purchased it from Pharmacy Innovations. Those with medical conditions requiring hormone therapy are at higher risk.
Check for the product name 'Estradiol 0.05% OPH Solution' on the label. It was sold by Pharmacy Innovations at their Erie, PA location. The recall was issued on October 21, 2022.
Look for the product name 'Estradiol 0.05% OPH Solution' on the label.
The FDA found unsanitary conditions at the manufacturing facility, which could lead to contamination risks.
The recall record does not specify a remedy.
Check the product label for 'Estradiol 0.05% OPH Solution' and verify it was sold by Pharmacy Innovations at their Erie, PA location.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0205-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0205-2023 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.
