Pharmacy Innovations recalls Ceftazidime Intravitreal vials due to insanitary conditions found during FDA inspection. This may lead to contamination risks for patients using the medication.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Ceftazidime Intravitreal vials because FDA inspections found unsanitary conditions at their facility. This could mean the medication might be contaminated, posing a risk to patients who use it.
FDA inspections identified unsanitary conditions at Pharmacy Innovations' facility. This could lead to contamination of the medication, potentially causing infections or other health issues for patients.
Patients prescribed Ceftazidime Intravitreal injections by healthcare providers. Those using the medication at home for eye infections may be at risk.
Check for the product name 'Ceftazidime Intravitreal (1ML vial) 22.5 MG/ML(2.25MG/0.1ML) Injectable' from Pharmacy Innovations. The product was sold starting from the facility address in Erie, PA.
Verify the product name and manufacturer to confirm if it's part of this recall.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination risks.
Check for the product name 'Ceftazidime Intravitreal (1ML vial) 22.5 MG/ML(2.25MG/0.1ML) Injectable' from Pharmacy Innovations.
The recall record does not specify a remedy, so contact Pharmacy Innovations 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-0197-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0197-2023 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.
