Pharmacy Innovations recalls NADH 10mg/ml injectable (Rx only) due to FDA-identified insanitary conditions. This may pose sterility risks. Affected products were sold in Erie, PA.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling NADH 10mg/ml injectable vials because FDA inspections found unsanitary conditions at their facility. This could lead to contamination risks for patients using the medication.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of proper sanitation could lead to contamination of the injectable medication, potentially causing infections or other health issues.
Prescription drug users who received NADH 10mg/ml injectable vials from Pharmacy Innovations in Erie, PA. Patients with medical conditions requiring this medication are most at risk.
Check for NADH 10mg/ml (10ml vial) injectable products labeled as 'Rx Only' from Pharmacy Innovations. These were sold in Erie, PA starting from the date of the FDA inspection.
Identify if your NADH 10mg/ml (10ml vial) injectable is from Pharmacy Innovations in Erie, PA.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination risks.
The recall notice does not specify a remedy.
Check for NADH 10mg/ml (10ml vial) injectable products labeled 'Rx Only' from 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-0225-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0225-2023 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.