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

Rad Health Inc. Rad Jaw Capsules recalled by NutraCap Labs

NutraCap Labs is recalling Rad Health Inc. Rad Jaw 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 #2108321 EXP DATE 08/2023 LOT #2105041 EXP DATE 05/2023

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-0478-2022
FDA event ID: 89000
Recalling firm: NutraCap Labs, Norcross, GA
Brand: Rad Health
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

Rad Health Inc. Rad Jaw Capsules 120ct Bottles UPC CODE 1 95893 50782 5

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 Rad Health Inc. Rad Jaw Capsules recalled?

Yes. NutraCap Labs recalled Rad Health Inc. Rad Jaw Capsules on 9 Nov 2021. The recall is Class I and its status is Terminated. Recall number F-0478-2022.

Why was it recalled?

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

Which lots are affected?

LOT #2108321 EXP DATE 08/2023 LOT #2105041 EXP DATE 05/2023

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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