Pharmacy Innovations recalls methylcobalamin injectables due to FDA finding of insanitary conditions at manufacturing facility. Products may not be sterile, posing infection risk.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling several methylcobalamin injectable products because an FDA inspection found unsanitary conditions at their facility. This could mean the products are not sterile and might cause infections if used.
The FDA found unsanitary conditions at Pharmacy Innovations' facility during an inspection. This means the injectables might not be sterile, which could lead to infections if used.
People who have received these methylcobalamin injectables for medical use are affected. Those with medical conditions requiring injections are most at risk.
Check for the product names: Methylcobalamin 12.5mg/ml (1ml vial), 25mg/ml (1.2ml vial), 3mg/ml (1ml vial), 5mg/ml (0.2ml vial), or 5mg/ml (1ml vial). These are prescription-only products sold by Pharmacy Innovations in Erie, PA.
Look for the specific product names and vial sizes listed in the recall notice.
The FDA found unsanitary conditions at Pharmacy Innovations' facility during an inspection, which could mean the products are not sterile.
The recall notice does not specify a remedy, so check with Pharmacy Innovations or your healthcare provider for guidance.
The recall indicates a risk of not being sterile, so they should not be used until the recall is resolved.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0222-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0222-2023 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.
