Check the Batch
Class IIITerminated in FDA datasetRecall initiated Jan 18, 2013

MET-Rx EXTREME NOS PUMPED WATERMELON Naturally and Artificially Flavored DIETARY SUPPLEMENT, 20…

Recalling firm: NBTY Inc.

Why it was recalled

The color, odor, and taste of the products are changing and do not meet the firm's high quality standards. This is an issue of commercial spoilage.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Dec 2, 2013.

Check your package

Compare the exact product and package details with the label you have.

ProductMET-Rx EXTREME NOS PUMPED WATERMELON Naturally and Artificially Flavored DIETARY SUPPLEMENT, 20 FL. OZ. (1.25 PT) (591 mL), UPC 7 49826 27603 8, Label Revision 02C, Item Number 27603 (Bottle) Item Number 27604 (case) --- Manufactured in the USA by MET-Rx Nutrition, Inc. Boca Raton, FL 33487
Package size20 FL. OZ
UPC749826276038

FDA code information

Lot 460259, exp. 10/31/2013; Lot 464764, exp. 12/31/2013

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

MET-Rx EXTREME NOS PUMPED WATERMELON Naturally and Artificially Flavored DIETARY SUPPLEMENT, 20 FL. OZ. (1.25 PT) (591 mL), UPC 7 49826 27603 8, Label Revision 02C, Item Number 27603 (Bottle) Item Number 27604 (case) --- Manufactured in the USA by MET-Rx Nutrition, Inc. Boca Raton, FL 33487

Extracted codes and context

TypeCode / valueContext
UPC749826276038nd Artificially Flavored DIETARY SUPPLEMENT, 20 FL. OZ. (1.25 PT) (591 mL), UPC 7 49826 27603 8, Label Revision 02C, Item Number 27603 (Bottle) Item Number 27604 (case) --- Manufactured in the USA by MET-Rx Nutritio

Original FDA recall reason

The color, odor, and taste of the products are changing and do not meet the firm's high quality standards. This is an issue of commercial spoilage.

Recall details

Recall number
F-1223-2013
Event ID
64422
FDA status
Terminated
Initiated
Jan 18, 2013
Reported
Mar 27, 2013
Classified
Mar 18, 2013
Terminated
Dec 2, 2013
Quantity
28,068 bottles
Location
Bohemia, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide

FDA source record · F-1223-2013

Data updated September 16, 2026. View official FDA data ↗

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