Reported Apr 17, 2019 · Terminated

PAPAVERINE-PHENTOLAMINE-PGE1 22-0.8 MG-8 MCG/ML* INJECTABLE, (a) 5ml (b) 10ml, (c) 6ml, penile injection, Professional…

Health Solutions Pharmacy Center Inc. dba Professional Compounding Pharmacy

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Health Solutions Pharmacy Center Inc dba Professional Compounding Pharmacy · 996 Nw Circle Blvd Ste 105 · Corvallis, OR · 97330-1485

Is this the product you have?

  • PAPAVERINE-PHENTOLAMINE-PGE1 22-0.8 MG-8 MCG/ML* INJECTABLE, (a) 5ml (b) 10ml, (c) 6ml, penile injection, Professional Compounding Pharmacy, 996 NW Circle Blvd. #105 Corvallis, OR 97330
Lot codes and dates
  • Lot
    • (a) 18092018@52
    • 01102018@9
    • 05102018@36
    • 08102018@11
    • 102018@9
    • 01102018@9
    • 01102018@9
    • 03102018@27
    • 12102018@18
    • 01102018@9
    • 12102018@18
    • 12102018@18
    • 17102018@15
    • 12102018@18
    • 2102018@18
    • 22102018@31
    • 30102018@22
    • 29102018@9
    • 29102018@9 29102018@9
    • 29102018@9
    • 12102018@18
    • 21112018@38
    • 21112018@38
    • 21112018@38
    • 21112018@38
    • 21112018@38
    • 21112018@38
    • 11122018@7
    • 11122018@7
    • 28122018@11
    • 28122018@11
    • 28122018@11
    • 03012019@17
    • 03012019@17
    • 03012019@17
    • 08012019@21
    • 08012019@21
    • 28082018@16 28082018@16
    • 28082018@16
    • 14092018@28
    • 14092018@28
    • 4092018@28
    • 14092018@28
    • 18092018@52
    • 18092018@52
    • 8092018@52
    • 18092018@52
    • 18092018@52
    • (b) 29102018@9
    • 03012019@17
    • 14092018@28
    • (c) 11012019@64
    • 11012019@64
    • 11012019@64
    • 05022019@27
    • 5022019@27
    • 06022019@6
    • 06022019@6
    • distributed between 09-01-2018 to 02-20-2019
Amount recalled
64 prescriptions 5, 10, 6 mL injections

This recall covers 25 products

The agency filed one notice per product. You are reading one of them; the other 24 are below.

12 more are in the archive.

Where it was sold

Why it was recalled

Lack of Processing Controls: Insanitary conditions observed during compounding of sterile drugs during recent FDA Inspection.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jul 23, 2020 · Data as of Sep 19, 5:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.