CLASS I Food recall · Reported 19 Jan 2022 · FDA Enforcement Report
Vyce World Nutrition Bed Burn Capsules Bottle NO recalled
NutraCap Labs is recalling Vyce World Nutrition Bed Burn Capsules Bottle NO, distributed in 26 states. The recall was initiated on 9 Nov 2021 and the FDA has classified it as Class I.
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-0499-2022
- FDA event ID
- 89000
- Recalling firm
- NutraCap Labs, Norcross, GA
- Brand
- Vyce World
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 9 Nov 2021
- FDA classified
- 11 Jan 2022
- Reported
- 19 Jan 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Undeclared Milk
- Product category
- Fish
Timeline
| 9 Nov 2021 | Recall initiated by company | |
| 11 Jan 2022 | Classified by FDA | +63 days |
| 19 Jan 2022 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
During an FDA investigation the firm was notified that the product contains undeclared milk.
Product as listed by the FDA
Vyce World Nutrition Bed Burn Capsules 60ct Bottle NO UPC CODE
Where it was distributed
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA & WA.
AlabamaArkansasArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIdahoIllinoisIndianaKentuckyLouisianaMarylandMinnesotaNorth CarolinaNew JerseyNevadaNew YorkOhio
Questions about this recall
Is Vyce World Nutrition Bed Burn Capsules Bottle NO recalled?
Yes. NutraCap Labs recalled Vyce World Nutrition Bed Burn Capsules Bottle NO on 9 Nov 2021. The recall is Class I and its status is Terminated. Recall number F-0499-2022.
Why was it recalled?
During an FDA investigation the firm was notified that the product contains undeclared milk.
Which lots are affected?
LOT #2101178 EXP DATE 01/2023
Where was it sold?
Product was shipped to the following states: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MD, MN, NC, NJ, NV, NY, OH, OR, SC, TN, TX, VA & WA.
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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