CLASS II Food recall · Reported 16 Apr 2014 · FDA Enforcement Report
vitacost Men's Passion Booster, Premium Formula Dietary Supplement recalled
Nature's Value is recalling vitacost Men's Passion Booster, Premium Formula Dietary Supplement, distributed in Florida. The recall was initiated on 24 Feb 2014 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1762-2014
- FDA event ID
- 67632
- Recalling firm
- Nature's Value, Coram, NY
- Brand
- vitacost
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 24 Feb 2014
- FDA classified
- 10 Apr 2014
- Reported
- 16 Apr 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Dietary Supplements
Timeline
| 24 Feb 2014 | Recall initiated by company | |
| 10 Apr 2014 | Classified by FDA | +45 days |
| 16 Apr 2014 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
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
Where it was distributed
Florida
Questions about this recall
Is vitacost Men's Passion Booster, Premium Formula Dietary Supplement recalled?
Yes. Nature's Value recalled vitacost Men's Passion Booster, Premium Formula Dietary Supplement on 24 Feb 2014. The recall is Class II and its status is Terminated. Recall number F-1762-2014.
Why was it 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 lots are affected?
30 capsules: Lot Nos. 1768600, 1783100, 2091200, 1979500; -- 120 capsules: Lot Nos. 1768600, 1646900, 1783100, 2050500, 2091200, 1979500
Where was it sold?
Florida
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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