Pharmacy Innovations recalls Dexamethasone injections due to FDA finding insanitary conditions at manufacturing facility. Products may cause infection if used.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling three types of dexamethasone injections because FDA inspections found unsanitary conditions at their facility. Using these products could lead to infections if they are not sterile.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This means the injections might not be sterile, which could cause infections if used.
People who have received the recalled dexamethasone injections from Pharmacy Innovations. Those with medical conditions requiring injections are at higher risk.
Check for the product names: Dexamethasone 16mg/ml (3ml vial) injectable, Dexamethasone 24mg/ml injectable, or Dexamethasone-PF-0.1% (1ml dropper) ophthalmic solution. These were sold by Pharmacy Innovations in Erie, PA.
Look for the product names and manufacturer on the packaging to confirm if it is recalled.
FDA inspections found insanitary conditions at Pharmacy Innovations' facility, which could mean the injections are not sterile.
The recall record does not specify a remedy, so check with Pharmacy Innovations or your healthcare provider.
The recall indicates a risk of infection due to potential lack of sterility, so it is not safe to use without confirming it is recalled.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0201-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0201-2023 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.
