Drug & medication recalls Moderate risk

Neostigmine Methylsulfate 5 mg/ Injection Solution 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 Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, C…
Recall number
D-0200-2017
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

Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15

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