Phenylephrine PF recalled over sterility concerns
- Recall date
- September 12, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- US Compounding Inc recalls Phenylephrine PF (1 mg/10 mL), 10 mL Single Use Syringe, For IV Use, Rx only, Compounded by US Compounding Pharmacy, Co…
- Recall number
- D-0276-2016
- FDA classification
- Class II
- Brand / firm
- US Compounding Inc
- Sold / distributed
- Nationwide
Why it was recalled
Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Phenylephrine PF (1 mg/10 mL), 10 mL Single Use Syringe, For IV Use, Rx only, Compounded by US Compounding Pharmacy, Conway, Arkansas, 72032, NDC 62295-3159-07
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