Pharmacy Innovations recalls Hydroxocobalamin 25MG/:2ML vials due to FDA-identified insanitary conditions causing potential contamination risks.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Hydroxocobalamin 25MG/ML (2ML vial) injectables because FDA inspections found unsanitary conditions at their facility. This could lead to contamination risks for patients using the medication.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of sterility could lead to contamination of the injectable medication, potentially causing infections or other health issues for patients.
Patients prescribed Hydroxocobalamin 25MG/ML (2ML vial) injectables by pharmacies or healthcare providers. Those using the product without proper sterility checks are at higher risk.
Check for Hydroxocobalamin 25MG/ML (2ML vial) injectables labeled as Pharmacy Innovations, 2936 W 17th St., Erie, PA. The product was distributed starting from the date mentioned in the recall notice.
Verify the product label matches Hydroxocobalamin 25MG/ML (2ML vial) with Pharmacy Innovations as the manufacturer.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination risks for patients using the medication.
Check for Hydroxocobalamin 25MG/ML (2ML vial) injectables labeled as Pharmacy Innovations, 2936 W 17th St., Erie, PA.
The recall record does not specify a remedy, so contact Pharmacy Innovations directly for guidance.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0187-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0187-2023 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.
