Pharmacy Innovations recalls polidocanol 50mg/ml (5%) 30ml vials due to FDA finding insanitary conditions. Stop using if you have this prescription drug.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling polidocanol 50mg/ml (5%) 30ml vials because an FDA inspection found unsanitary conditions at their facility. This could lead to infections if the medication is used.
The FDA found unsanitary conditions at Pharmacy Innovations' facility. This means the vials might not be sterile, which could cause infections if injected.
Prescription drug users who have the polidocanol 50mg/ml (5%) 30ml vials from Pharmacy Innovations. People using this medication for medical treatment are most at risk.
Check for polidocanol 50mg/ml (5%) 30ml vials labeled as Pharmacy Innovations. These were sold in Erie, PA, and are prescription-only.
Look for polidocanol 50mg/ml (5%) 30ml vials from Pharmacy Innovations.
The FDA found unsanitary conditions at Pharmacy Innovations' facility, which could lead to infections if the medication is used.
Check for polidocanol 50mg/ml (5%) 30ml vials labeled as Pharmacy Innovations.
The recall record does not specify a remedy, so contact Pharmacy Innovations 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-0231-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0231-2023 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.
