Pharmacy Innovations recalls specific vitamin injectable products due to FDA-identified unsanitary facility conditions. Consumers should check product labels for the listed formulations and contact the company for details.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled several vitamin injectable products because an FDA inspection found unsanitary conditions at their manufacturing facility. This could lead to contamination and potential infection if the products are used.
The FDA found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination of the products. This contamination might cause infections if the injectable products are used.
People who have purchased or received these vitamin injectable products from Pharmacy Innovations in the United States. Those with medical conditions requiring injections are at higher risk.
Check for the product names listed in the recall: METHION/INOSIT/CHOLINE/CYANOCOBAL 25MG/50MG/50MG/1MG/ML (1ML VIAL) INJECTABLE, METHION/INOSIT/CHOLINE/METHYLCOBAL 15MG/50MG/100MG/1MG/ML (1ML VIAL) INJECTABLE, or METHION/INOSIT/CHOLINE/RIBOFLA/NIACINAMIDE/PYRIDOX/ASCORBIC ACID 15.625MG/31.25MG/31.25MG/6.25MG/62.5MG/6.25MG/62.5MG/ML (1ML VIAL) INJECTABLE. These products are prescription-only.
Look for the specific product names and labels mentioned in the recall notice to confirm if your product is affected.
The FDA found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination of the products.
The recall notice does not specify a remedy, so check with Pharmacy Innovations for further instructions.
The recall indicates a risk of contamination due to unsanitary conditions, so they should not be used until the manufacturer provides further instructions.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0220-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0220-2023 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.
