Pharmacy Innovations recalls two vitamin D3 injectable products due to FDA-identified unsanitary conditions at their manufacturing facility. This could lead to contamination risks for users.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling two vitamin D3 injectable products because an FDA inspection found unsanitary conditions at their facility. This means the products could be contaminated, posing a health risk to users.
The FDA found unsanitary conditions at Pharmacy Innovations' manufacturing facility. This could lead to contamination of the vitamin D3 products, potentially causing infections or other health issues for users.
People who have purchased or received these vitamin D3 injectable products from Pharmacy Innovations. Those with medical conditions requiring vitamin D injections are at higher risk.
Check for the product names: Vitamin D3-AQUEOUS- 10,000IU/ML (1ML VIAL) INJECTABLE or Vitamin D3-PF-ETHYL OLEATE- 50,000IU/ML (1ML VIAL) INJECTABLE. These are prescription-only products sold by Pharmacy Innovations.
Look for the product names and check if they were purchased from Pharmacy Innovations.
The FDA found unsanitary conditions at Pharmacy Innovations' manufacturing facility, which could lead to contamination of the vitamin D3 products.
The recall record does not specify a remedy, so there is no action required beyond checking if you have the product.
The recall record indicates a risk of contamination due to unsanitary conditions, so it is not safe to use.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0242-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0242-2023 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.
