US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 26, 2017 (9 years ago)

Lactulose Solution, USP, 20 g/30 mL, dose cups delivers 30 mL packaged 50-unit dose cups…

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

Why it was recalled

Microbial contamination of non-sterile product: product failed Total Yeast/Mold Count specification.

What was recalled

Lactulose Solution, USP, 20 g/30 mL, dose cups delivers 30 mL packaged 50-unit dose cups per case, Manufactured by VistaPharm, Inc., Largo, FL 33771, NDC 66689-038-01

Recalling firm
VistaPharm, Inc.
NDC code
66689-038-01
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1053-2017

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.

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