Pharmacy Innovations recalls multiple testosterone injection products due to FDA findings of insanitary conditions at manufacturing facility. Products may contain contaminants that could cause infection.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled several testosterone injection products because FDA inspections found unsanitary conditions at their manufacturing facility. These products could be contaminated, posing a risk of infection if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This could lead to contamination of the products, potentially causing infections in users who receive the injections.
People who have received these testosterone injections from Pharmacy Innovations are affected. Those with medical conditions requiring injections are at higher risk of infection.
Check for the product names listed in the recall, including various testosterone injection formulations. Products were sold by Pharmacy Innovations at their location in Erie, PA.
Look for the specific product names and quantities listed in the recall notice.
FDA inspections found unsanitary conditions at Pharmacy Innovations' manufacturing facility, which could lead to contamination of the products.
Check the product labels for the specific testosterone injection formulations listed in the recall notice, including the quantities and formulations.
The recall notice 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-0238-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0238-2023 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.
