Severity
Low
LowClass IIITerminated
FDA Food recall · Reported March 27, 2013
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.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
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 FDA Food action (record #F-1224-2013) was formally reported on March 27, 2013, with the manufacturer initiating the action on January 18, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Nbty Inc. is listed as the recalling firm, operating out of Bohemia, NY. Federal records list the affected scope as 5412 bottles.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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.
Affected scope
5412 bottles
Related Recalls
6
0 from same agency
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
| 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? ▼
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. Recalled by Nbty Inc.. Units affected: 5412 bottles.
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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1224-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 27, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.