Pharmacy Innovations recalls multiple injectable medicine vials due to FDA finding insanitary conditions at manufacturing facility. Products contain PE1/PAPAV/PHEN and PHENT compounds at various concentrations. No remedy specified in recall notice.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled several injectable medicine vials that were produced at a facility with insanitary conditions. These products pose a risk of contamination that could lead to infections if used.
FDA inspections found unsanitary conditions at the manufacturing facility. This lack of proper sanitation could lead to contamination of the medicines, potentially causing infections when injected.
Patients who have received these injectable medicines from Pharmacy Innovations in Erie, PA. Healthcare providers using these products for medical treatments are at risk.
Check for vials labeled with PE1/PAPAV/PHEN or PHENT compounds at various concentrations (e.g., 20MCG/30MG/2MG/ML). These products were distributed in Erie, PA and were sold between 2022-10-03 and 2022-11-28.
Look for vials with PE1/PAPAV/PHEN or PHENT compounds at various concentrations listed in the recall notice.
FDA inspections found insanitary conditions at the manufacturing facility, which could lead to contamination of the medicines.
The recall notice does not specify a remedy, so check with Pharmacy Innovations for guidance.
Products were distributed between 2022-10-03 and 2022-11-28 based on the recall notice dates.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0228-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0228-2023 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.
