Pharmacy Innovations recalls Vitamin D3 injectable due to FDA finding unsanitary conditions at manufacturing facility. No remedy specified in official notice.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Vitamin D3 injectable products because FDA inspections found unsanitary conditions at their Erie, PA facility. This could pose a risk of infection from contaminated products.
FDA inspections found unsanitary conditions at the manufacturing facility. This could lead to contamination of the product, potentially causing infections if injected.
People who have received the recalled Vitamin D3 injectable from Pharmacy Innovations in Erie, PA. Those with medical conditions requiring injections are most at risk.
Check for the product name 'Cholecalciferol (Vitamin D3) 100,000U/ML Injectable' with the manufacturer Pharmacy Innovations. The products were sold in Erie, PA.
Look for the product name and manufacturer on the label to confirm if it matches the recalled items.
The official notice does not specify any remedy.
FDA inspections found unsanitary conditions at the manufacturing facility.
People with medical conditions requiring injections are most at risk.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0198-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0198-2023 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.
