Pharmacy Innovations recalls Apom: 2mg/ml injectable vials due to FDA-identified insanitary conditions. No remedy specified in official notice.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations is recalling Apomorphine HCL 2MG/ML (10ML vial) injectables because FDA found unsanitary conditions at their facility. This could lead to infections if the product is used.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility. This lack of sterility could cause infections if the injectable product is used.
People with prescriptions for Apomorphine HCL 2MG/ML vials from Pharmacy Innovations in Erie, PA. Those using the product for medical purposes are at risk of infection.
Check for Apomorphine HCL 2MG/ML (10ML vial) injectables labeled 'Pharmacy Innovations' from Erie, PA. The recall was issued on November 8, 2022.
Verify the product name, brand, and location as listed in the recall notice.
The official notice does not specify a remedy.
FDA inspections found unsanitary conditions at the facility, which could lead to infections if the product is used.
Look for Apomorphine HCL 2MG/ML (10ML vial) injectables from Pharmacy Innovations in Erie, PA.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0193-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0193-2023 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.
