Pharmacy Innovations recalls specific estradiol injectables due to FDA finding of insanitary conditions at manufacturing facility. Products may not be sterile, posing infection risks. Consumers should contact pharmacy for details.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling several estradiol injectable products because FDA inspections found unsanitary conditions at their facility. This means the products could be contaminated and cause infections if used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This could mean the injectables are not sterile, which might lead to infections if used. The hazard is related to the manufacturing process, not the product itself.
People who have received these specific estradiol injectable products for medical treatment. Those with hormone therapy or related conditions are at risk if they use the recalled products.
Check for the product names: ESTRADIOL CYP/TEST CYP-SS OIL-2MG/50MG/ML (1.5ML VIAL), ESTRADIOL CYP/TEST CYP-SS OIL-2MG/25MG/ML (1ML VIAL), and similar estradiol injectables. These were sold by Pharmacy Innovations in Erie, PA.
Look for the specific product names and vial sizes listed in the recall notice.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could mean the products are not sterile.
The recall notice does not specify a remedy, so contact Pharmacy Innovations directly for guidance.
Yes: ESTRADIOL CYP/TEST CYP-SS OIL-2MG/50MG/ML (1.5ML VIAL), ESTRADIOL CYP/TEST CYP-SS OIL-2MG/25MG/ML (1ML VIAL), and similar estradiol injectables.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0206-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0206-2023 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.
