US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 2, 2016 (10 years ago)

PAPA/PHEN/PROST (papverine/phentolamine/prostaglandin) 18 mg/0.6 mg/0.006 mg/mL…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility: product produced on a day there was an excursion in environmental monitoring data.

What was recalled

PAPA/PHEN/PROST (papverine/phentolamine/prostaglandin) 18 mg/0.6 mg/0.006 mg/mL Injection, 1 mL vials, Fallon Wellness Pharmacy LLC, 1057 Troy-Schenectady Rd, Latham, NY 12110.

Recalling firm
Fallon Wellness Pharmacy, L.L.C.
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0173-2017

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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