MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored DIETARY SUPPLEMENT, 20 FL. OZ. (1.25 PT) (591 mL), UPC 7 49826 35909 0, Label Revision 01C, Item Number 35909 (Bottle) Item Number 35910 (case) --- Manufactured in the USA by MET-Rx Nutrition, Inc. Boca Raton, FL 33487

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 #: F-1224-2013
Affected scope: 5412 bottles
Initiated: January 18, 2013

Compiled from official public sources by the publisher. · Updated September 2026

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Nbty Inc. recalled MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored DIETARY SUPPLE… - a low-severity action.

MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored DIETARY SUPPLE… was recalled by Nbty Inc. in March 27, 2013. Reason: The color, odor, and taste of the products are changing and do not meet the firm's high quality standards. T…. Check the official notice for the remedy. Verify recall #F-1224-2013 with the FDA Food before acting.

The recall

Nbty Inc. issued this low-severity FDA Food recall-The color, odor, and taste of the products are changing and do not meet the firm's high quality standards. T….

Low
severity level: Class III
classification: March 27, 2013
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1224-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored DIETARY SUPPLEMENT, 20 FL. OZ. (1.25 PT) (591 mL), UPC 7 49826 35909 0, Label Revision 01C, Item Number 35909 (Bottle) Item Number 35910 (case) --- Manufactured in the USA by MET-Rx Nutrition, Inc. Boca Raton, FL 33487

Reason for recall

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 Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	F-1224-2013
Date reported	March 27, 2013
Date initiated	January 18, 2013
Recalling firm	Nbty Inc.
Firm location	Bohemia, NY
Affected scope	5412 bottles
Distribution	Nationwide

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-1224-2013) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product 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.

Which agency issued this recall? ▼

This recall was issued by the FDA Food on March 27, 2013. Severity: Low. Recall number: F-1224-2013.

Where was the recalled product distributed? ▼

Distribution: Nationwide.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

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Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

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This recall: FDA Food, reported March 27, 2013. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026