Pharmacy Innovations recalls methylcobalamin injectable products due to FDA-identified insanitary conditions at manufacturing facility. Products may contain contaminants that could cause infection if used.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling methylcobalamin injectable products (1mg/ml, 3mg/ml, and 5mg/ml vials) because FDA inspections found unsanitary conditions at their facility. These products could be contaminated and pose a risk of infection if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' manufacturing facility. This could lead to contaminated products that may cause infections when injected.
People who have received the recalled methylcobalamin injectable products for medical use are affected. Patients using these products for treatment are at risk of infection.
Check for methylcobalamin injectable vials labeled 1mg/ml, 3mg/ml, or 5mg/ml. These products were sold by Pharmacy Innovations in Erie, PA, starting around October 2022.
Look for vials labeled with methylcobalamin 1mg/ml, 3mg/ml, or 5mg/ml for injectable use.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contaminated products.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the product.
The recall states a risk of contamination that could cause infection, but the record does not mention serious injury or death.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0188-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0188-2023 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.
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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.
