FDA recall record

National Vitamin Co Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each, 100 recall — FDA D-0568-2016

Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as Docusate Calcium 240mg.

Class IIIclassification
D-0568-2016official record ID
Jan 20, 2016report date

Recall record at a glance

Official recordD-0568-2016
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmNational Vitamin Co Inc.
Report dateJan 20, 2016
Recall initiation dateDec 18, 2015
Quantity29,827 bottles
LocationCasa Grande, AZ, United States

Official product description

Life-Line DOCUSATE CALCIUM Sodium Free STOOL SOFTENER 240 mg each, 100 softgels per bottle. UPC 0-79854-95005-2 Manufactured and Distributed by: NATIONAL VITAMIN COMPANY Casa Grande, AZ 85122. NDC 54629-0640-01

Why the product was recalled

Labeling: Label mix-up. Docusate Sodium 100mg Softgels were mislabeled as Docusate Calcium 240mg.

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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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