Papaverine/phentolamine/prostaglandin 30/1/0 recalled over sterility concerns
- Recall date
- March 17, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Fallon Wellness Pharmacy, L.L.C. recalls Papaverine/phentolamine/prostaglandin 30/1/0.02 mg/mL Injection, Fallon Wellness Pharmacy, L.L.C., Latham, NY 12110
- Recall number
- D-1070-2015
- FDA classification
- Class II
- Brand / firm
- Fallon Wellness Pharmacy, L.L.C.
- Sold / distributed
- New York
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
Papaverine/phentolamine/prostaglandin 30/1/0.02 mg/mL Injection, Fallon Wellness Pharmacy, L.L.C., Latham, NY 12110
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