Wise Pharmacy recalls specific compounded injectable medication (Papaverine/Phentolamine/Alprostadil) due to lack of processing controls. Affected lots expired by 2019.
Lack of Processing Controls
Wise Pharmacy has recalled a compounded injectable medication that may have been made without proper processing controls. This could pose a risk to patients using it for medical treatment.
The medication was compounded without proper processing controls, which could lead to contamination or incorrect dosing. This is a serious issue for patients using it for medical treatment.
Patients prescribed this compounded medication by a healthcare provider in the United States. Those who received the medication from Wise Pharmacy in Littleton, CO between the specified lot dates are most at risk.
Check the vial label for the product name and lot number. The affected lots are 6176N (expires 8/30/2019) and 7162N (expires 10/20/2019).
Look for the lot numbers 6176N or 7162N on the vial label.
The recall record does not state whether the medication is safe to use. It mentions a lack of processing controls but does not specify if the medication is safe or unsafe.
The recall record does not provide specific action steps for affected individuals beyond checking the lot number.
The recall record does not mention any replacement or remedy options.
We’ve drafted a message you can send Wise Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-1576-2019 — Wise Pharmacy Wise Pharmacy Hello, I own a Wise Pharmacy that is covered by recall D-1576-2019 from Wise Pharmacy. 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.
