US Drug Recall Register
Class II · Moderate risk Terminated Initiated Nov 18, 2016 (10 years ago)

Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose…

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

Why it was recalled

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

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

Recalling firm
Cantrell Drug Company
NDC code
52533-046-15
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0200-2017

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.

Other Methyl recalls

See all