Pharmacy Innovations recalls multiple vitamin injectable products manufactured at a facility with insanitary conditions. The FDA found lack of sterility assurance, posing potential infection risks. Consumers should contact the company for details.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled several injectable vitamin products because the manufacturing facility had insanitary conditions. This could lead to infections if the products are used, as the FDA found a lack of sterility assurance during inspection.
The FDA inspection found that the facility had insanitary conditions, which means the products might not be sterile. If these injectable vitamins are used, there is a risk of infection because the products could have been contaminated during manufacturing.
People who have purchased or received these injectable vitamin products from Pharmacy Innovations. Those using the products for medical purposes are at higher risk due to potential infection.
Check for the product names: THIAMINE/RIBOFLA/NIACINAMI/DEXPANTH/PYRIDOX/HYDROXYCOBAL 25MG/25MG/25MG/25MG/25MG/20MG/ML (3ML VIAL) INJECTABLE or similar variants. The products were sold by Pharmacy Innovations in Erie, PA, and were manufactured around late 2022.
Reach out to Pharmacy Innovations at 2936 W 17th St., Erie, PA for specific product details and instructions.
The FDA found insanitary conditions at the manufacturing facility, leading to a lack of sterility assurance in the products.
The products were recalled due to potential contamination risks, so they should not be used until the company provides further instructions.
Look for the product names listed in the recall notice, which include specific vitamin combinations and vial sizes. The products were sold by Pharmacy Innovations in Erie, PA around late 2022.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0239-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0239-2023 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.
