Pharmacy Innovations recalls Dutasteride 0.1% injectable vials due to FDA-identified insanitary conditions at manufacturing facility. No remedy specified in official notice.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Dutasteride 0.1% (1.5mL) injectable vials because FDA inspections found unsanitary conditions at their Erie, PA facility. This could lead to infections if the medication is used without proper sterility.
FDA inspections found unsanitary conditions at Pharmacy Innovations' manufacturing facility. This means the injectable vials might not be sterile, potentially causing infections if used.
People with prescriptions for Dutasteride 0.1% injectable vials from Pharmacy Innovations in Erie, PA. Those using the medication for conditions like prostate cancer or male pattern baldness are most at risk.
Check for Dutasteride 0.1% (1.5mL) vials labeled 'Pharmacy Innovations' from Erie, PA. The recall includes vials produced between October 12, 2022, and November 9, 2022.
Look for the product name, manufacturer, and production dates on the vial label.
The FDA found unsanitary conditions at the manufacturing facility, so the product may not be sterile and could cause infections. Do not use.
The official recall notice does not specify a remedy, so contact Pharmacy Innovations directly for guidance.
The vials were produced between October 12, 2022, and November 9, 2022, as indicated in the recall notice.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0185-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0185-2023 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.
