PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported April 16, 2014

vitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, ITEM # NSI 3004713, UPC 8 35003 00471 3, and 120 CAPSULES, ITEM # NSI 3009473, UPC 8 35003 00947 3 --- Manufactured for Vitacost Lexington, NC 27295

The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier since the lot was found to contain a compound other than L-Citrulline.

Recall #
F-1762-2014
Affected scope
30 capsules: 2169 bottles; 120 capsules: 2052 bottles
Initiated
February 24, 2014
Verify with FDA Food →
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Nature's Value Inc. recalled vitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, IT… - a moderate-severity action.

vitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, IT… was recalled by Nature's Value Inc. in April 16, 2014. Reason: The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier…. Check the official notice for the remedy. Verify recall #F-1762-2014 with the FDA Food before acting.

The recall

Nature's Value Inc. issued this moderate-severity FDA Food recall-The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier….

Moderate
severity level
Class II
classification
April 16, 2014
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1762-2014 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, 5 from FDA Food - 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.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,014 dietary supplements recalls on record

0100200300400 20072010201320162019202220252026 21
Severity1906864652High severity (most serious)Moderate severityLow severity
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 moderate severity.

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

Product description

vitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, ITEM # NSI 3004713, UPC 8 35003 00471 3, and 120 CAPSULES, ITEM # NSI 3009473, UPC 8 35003 00947 3 --- Manufactured for Vitacost Lexington, NC 27295

Reason for recall

The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier since the lot was found to contain a compound other than L-Citrulline.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1762-2014
Date reported April 16, 2014
Date initiated February 24, 2014
Recalling firm Nature's Value Inc.
Firm location Coram, NY
Affected scope 30 capsules: 2169 bottles; 120 capsules: 2052 bottles
Distribution Florida

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-1762-2014) 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?
vitacost brand Men's Passion Booster, 30 Capsules, PREMIUM FORMULA DIETARY SUPPLEMENT, ITEM # NSI 3004713, UPC 8 35003 00471 3, and 120 CAPSULES, ITEM # NSI 3009473, UPC 8 35003 00947 3 --- Manufactured for Vitacost Lexington, NC 27295. Recalled by Nature's Value Inc.. Units affected: 30 capsules: 2169 bottles; 120 capsules: 2052 bottles.
Why was this product recalled?
The product was produced using bulk L-Citrulline lot # 121109 which was subsequently recalled by the supplier since the lot was found to contain a compound other than L-Citrulline.
Which agency issued this recall?
This recall was issued by the FDA Food on April 16, 2014. Severity: Moderate. Recall number: F-1762-2014.
Where was the recalled product distributed?
Distribution: Florida.
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

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Goody King Magnetic Building Cubes and Blocks Recalled Due … → · All Dietary Supplements recalls

This recall: FDA Food, reported April 16, 2014. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026