FDA recall record

Bumetanide Tablets USP 0.5 mg recall — FDA D-341-2014

Failed Moisture Limit; Out of Specification (OOS) results were obtained for moisture content during stability testing at the 12 month time point,…

Class IIIclassification
D-341-2014official record ID
Dec 18, 2013report date

Recall record at a glance

Official recordD-341-2014
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSandoz Inc.
Report dateDec 18, 2013
Recall initiation dateNov 6, 2013
Quantity11,496 bottles (100 count) and 62 bottles (500 count)
LocationWilson, NC, United States

Official product description

Bumetanide Tablets USP 0.5 mg. Rx Only, a) 100-count Bottle, b) 500-count Bottle, Sandoz Inc., Princeton, NJ 08540, NDC a) 0185-0128-01, b) 0185-0128-05

Why the product was recalled

Failed Moisture Limit; Out of Specification (OOS) results were obtained for moisture content during stability testing at the 12 month time point, controlled room temperature conditions.

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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