FDA recall record

VistaPharm Lactulose Solution, USP, 20 g/30 mL, dose cups delivers 30 mL packaged 50-unit recall — FDA D-1053-2017

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

Class IIclassification
D-1053-2017official record ID
Aug 9, 2017report date

Recall record at a glance

Official recordD-1053-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVistaPharm, Inc.
Report dateAug 9, 2017
Recall initiation dateJun 26, 2017
Quantity9945 cases
LocationLargo, FL, United States

Official product description

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

Why the product was recalled

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

Distribution information

CA, IL, LA, NH, OH, PA, SC

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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