Pharmacy Innovations recalls specific PAPAVERINE/PHENTOLAMINE injectable vials due to FDA finding of insanitary conditions at manufacturing facility. No remedy specified in recall notice.
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Pharmacy Innovations has recalled several PAPAVERINE/PHENTOLAMINE injectable vials because an FDA inspection found unsanitary conditions at their 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 injectable products, potentially causing infections if used.
People who have prescription PAPAVERINE/PHENTOLAMINE injectables from Pharmacy Innovations in Erie, PA. Healthcare providers and patients using these medications are most at risk.
Check for vials labeled PAPAVERINE/PHENTOLAMINE 30MG/0.5MG/ML, 30MG/1MG/ML, 30MG/2MG/ML, 30MG/3MG/ML, or 30MG/5MG/ML (1ML) in injectable form. These were sold by Pharmacy Innovations in Erie, PA.
Look for vials labeled with specific PAPAVERINE/PHENTOLAMINE concentrations (30MG/0.5MG/ML to 30MG/5MG/ML) in injectable form.
FDA inspections found unsanitary conditions at Pharmacy Innovations' facility, which could lead to contamination of the injectable products.
The recall notice does not specify a remedy, so check with Pharmacy Innovations or your healthcare provider for guidance.
The recall notice does not provide specific batch numbers or model numbers.
We’ve drafted a message you can send Pharmacy Innovations to request your refund or repair — edit it as you like.
Subject: Recall D-0226-2023 — Pharmacy Innovations Pharmacy Innovations Hello, I own a Pharmacy Innovations that is covered by recall D-0226-2023 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.
