US Drug Recall Register
Class I · High risk Terminated Initiated Aug 21, 2015 (11 years ago)

Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b)…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Subpotent Drug

What was recalled

Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453

Recalling firm
Cantrell Drug Company
NDC code
52533-010-45
Origin
AR, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1153-2016

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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