Pharmacy Innovations recalls a specific injectable vitamin blend due to FDA finding unsanitary conditions at the manufacturing facility.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling a 1mL injectable vitamin blend (Dexpanthenol/Pyridoxine/Hydroxocobalamin) because FDA inspections found unsanitary conditions at their Erie, PA facility. This could lead to infections if the product is used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' manufacturing facility. This could mean the product isn't sterile, potentially causing infections if injected. The product is only for prescription use.
Prescription patients who received this specific injectable vitamin blend from Pharmacy Innovations. Healthcare providers using this product are most at risk due to the injectable nature.
Look for the product name 'Dexpanthenol/Pyridoxine/Hydroxocobalamin-PF- 250MG/100MG/1MG/ML (1ML vial)' on the label. It was sold in Erie, PA and distributed starting around October 2022.
Verify the product name and dosage on the label to confirm it matches the recalled item.
The FDA found unsanitary conditions at the manufacturing facility, so the product may not be sterile. Do not use it.
The recall record does not mention a replacement or remedy.
The product was distributed starting around October 2022 based on the distribution date in the record.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0202-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0202-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.