Pharmacy Innovations recalls two glycerin/lidocaine/epinephrine vials due to FDA finding of insanitary conditions at manufacturing facility. These injectable products may not be sterile and could cause infections if used.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled two types of glycerin/lidocaine/epinephrine vials after FDA found the facility had insanitary conditions. Using these vials could lead to infections because they might not be sterile.
The FDA found that the manufacturing facility had insanitary conditions. This means the vials might not be sterile, which could lead to infections if used for injections.
People who own or use these injectable vials for medical purposes are affected. Those with medical conditions requiring these medications are at higher risk.
Check for vials labeled 'GLYCERIN/LIDOCAINE HCL/EPINEPHRINE 31%(V/V)/0.17%/0.00017% (10ML VIALS)' or 'GLYCERIN/LIDOCAINE HCL/EPINEPHRINE 48.7%(W/V)/0.67%/0.00067% (10ML VIAL)'. These were sold by Pharmacy Innovations in Erie, PA.
Look for the specific product names and concentrations listed in the recall notice.
The FDA found insanitary conditions at the manufacturing facility, which could mean the vials are not sterile.
The recall notice does not specify a remedy, so check with Pharmacy Innovations or your healthcare provider for guidance.
The recall states a risk of infection due to potential lack of sterility, but does not mention serious injury.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0213-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0213-2023 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.
