Family Pharmacy of Statesville recalls Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 mg/0.5 mg injectable vials due to lack of sterility assurance. This medication is prescription-only and may pose infection risks if used.
Lack of Assurance of Sterility
Family Pharmacy of Statesville is recalling Trimix injectable medication because it lacks sterility assurance. This could lead to infections if the medication is used without proper sterility.
The medication lacks assurance of sterility, meaning it could be contaminated with bacteria or other pathogens. If injected, this could cause serious infections or other health complications.
Prescription patients who have received this specific Trimix vial from Family Pharmacy of Statesville. Those using the medication for medical purposes are at risk of infection.
Check for the vial label indicating 'Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 mg/0.5 mg Injectable 5 mL' and the lot number '07212020' with a bud date of 9/4/2020. This medication is prescription-only and sold by Family Pharmacy of Statesville.
Look for the specific product label and lot number 07212020 with a bud date of 9/4/2020.
The recall states there is a lack of sterility assurance, so it may pose infection risks. Do not use this product.
Check for the vial label indicating 'Trimix (Alprostadil/Papaverine/Phentolamine) 20 mcg/30 mg/0.5 mg Injectable 5 mL' and the lot number 07212020 with a bud date of 9/4/2020.
The recall does not specify a remedy, so contact Family Pharmacy of Statesville for guidance.
We’ve drafted a message you can send Family Pharmacy of Statesville to request your refund or repair — edit it as you like.
Subject: Recall D-0660-2022 — Family Pharmacy of Statesville Family Pharmacy of Statesville Hello, I own a Family Pharmacy of Statesville that is covered by recall D-0660-2022 from Family Pharmacy of Statesville. 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.
