Pharmacy Innovations recalls magnesium chloride hexahydrate injectable due to FDA finding 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 magnesium chloride hexahydrate injectable products because FDA inspections found unsanitary conditions at their facility. This could mean the products are not sterile and might cause infections if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of proper sanitation could lead to the injectable products not being sterile, increasing infection risk during medical use.
People with prescriptions for this injectable magnesium chloride solution. Those using it for medical purposes are at risk of infection.
Check for the product name 'MAGNESIUM CHLORIDE HEXAHYDRATE-PF- 200MG/ML (5ML VIAL) INJECTABLE' with the manufacturer 'Pharmacy Innovations' from their Erie, PA address. This product was sold starting from the date in the recall notice.
Look for the product name and manufacturer address listed in the recall notice to confirm if your product is affected.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could mean the product is not sterile.
The recall notice does not specify a remedy, so check the product details to confirm if it's affected and contact Pharmacy Innovations for further instructions.
The recall states a lack of assurance of sterility, which could lead to infection, but the notice does not describe specific injury risks.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0219-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0219-2023 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.
