Pharmacy Innovations recalls specific injectable medication vials due to FDA finding of insanitary conditions at manufacturing facility. These vials may not be sterile and pose infection risks.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling certain injectable medication vials because FDA inspections found unsanitary conditions at their facility. This means the vials may not be sterile and could cause infections if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of sterility means the medication vials could be contaminated and cause infections if injected.
People who have received these specific injectable medication vials from Pharmacy Innovations. Those using the vials for medical treatment are most at risk of infection.
Check for vials labeled with the specific medication names and dosages: PE1/PAPAV/ATROP/CHLORPROM with concentrations like 7MCG/8.7MG/0.1MG/1.8MG/ML. These were sold by Pharmacy Innovations in Erie, PA.
Look for specific medication names and dosages on the vial label.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could mean the medication vials are not sterile.
The recall record does not specify a remedy, so check with Pharmacy Innovations or your healthcare provider for guidance.
Yes, the affected vials have specific dosages like 7MCG/8.7MG/0.1MG/1.8MG/ML and were sold by 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-0227-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0227-2023 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.
