First Pharma Associates LLC dba Riverpoint Pharmacy product recalled over sterility concerns
- Recall date
- June 26, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- First Pharma Associates LLC dba Riverpoint Pharmacy recalls PAP/PHEN/PGE1 30 mg/0.83mg/10mcg/mL Injection, 5 mL, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane,…
- Recall number
- D-1481-2019
- FDA classification
- Class II
- Brand / firm
- First Pharma Associates LLC dba Riverpoint Pharmacy
- Sold / distributed
- ID, WA only
Why it was recalled
Lack of Assurance of Sterility.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
PAP/PHEN/PGE1 30 mg/0.83mg/10mcg/mL Injection, 5 mL, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252
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