Drug & medication recalls Moderate risk

Phenylephrine HCl 1 mg/ in 0 recalled over sterility concerns

Recall date
November 18, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Cantrell Drug Company recalls Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Com…
Recall number
D-0185-2017
FDA classification
Class II
Brand / firm
Cantrell Drug Company
Sold / distributed
Nationwide

Why it was recalled

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

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 HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12

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