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

Dube Ortho & PT Capsules No recalled by NutraCap Labs

NutraCap Labs is recalling Dube Ortho & PT Capsules 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

Lot, batch or date codesLOT #2006159 EXP DATE 06/2022 LOT #2012121 EXP DATE 12/2022

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-0430-2022
FDA event ID: 89000
Recalling firm: NutraCap Labs, Norcross, GA
Brand: Dube Ortho
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

Dube Ortho & PT 144 Bottles Capsules 60ct 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.

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 Dube Ortho & PT Capsules No recalled?

Yes. NutraCap Labs recalled Dube Ortho & PT Capsules No on 9 Nov 2021. The recall is Class I and its status is Terminated. Recall number F-0430-2022.

Why was it recalled?

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

Which lots are affected?

LOT #2006159 EXP DATE 06/2022 LOT #2012121 EXP DATE 12/2022

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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