CLASS I Food recall · Reported 19 Jan 2022 · FDA Enforcement Report

ViVa/ViValife Joint Support Capsules recalled by NutraCap Labs

NutraCap Labs is recalling ViVa/ViValife Joint Support Capsules, distributed in 26 states. The recall was initiated on 9 Nov 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT #2107178 EXP DATE 07/2023

Quantity recalled80,169 various bottles and jars

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-0498-2022
FDA event ID: 89000
Recalling firm: NutraCap Labs, Norcross, GA
Brand: ViVa
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 Fish & Shellfish
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 shellfish.

Product as listed by the FDA

ViVa/ViValife Joint Support Capsules 90ct Bottle UPC CODE 1 95893 94873 4

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.

Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Idaho Illinois Indiana Kentucky Louisiana Maryland Minnesota North Carolina New Jersey Nevada New York Ohio

Questions about this recall

Is ViVa/ViValife Joint Support Capsules recalled?

Yes. NutraCap Labs recalled ViVa/ViValife Joint Support Capsules on 9 Nov 2021. The recall is Class I and its status is Terminated. Recall number F-0498-2022.

Why was it recalled?

During an FDA investigation the firm was notified that the product contains undeclared shellfish.

Which lots are affected?

LOT #2107178 EXP DATE 07/2023

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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