Class ITerminated in FDA datasetRecall initiated Nov 9, 2021

CFP (Clark Family Practice) Arthro 3000 Capsules 120ct

Recalling firm: NutraCap Labs LLC

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 21, 2024.

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ProductCFP (Clark Family Practice) Arthro 3000 Capsules 120ct UPC CODE 8 60004 06620 0
UPC860004066200

FDA code information

LOT #2110063 EXP DATE 10/2023 LOT #2007004 EXP DATE 07/2022

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Full FDA record and distribution details

Original product description

CFP (Clark Family Practice) Arthro 3000 Capsules 120ct UPC CODE 8 60004 06620 0

Extracted codes and context

TypeCode / valueContext
UPC860004066200CFP (Clark Family Practice) Arthro 3000 Capsules 120ct UPC CODE 8 60004 06620 0
lot2007004LOT #2110063 EXP DATE 10/2023 LOT #2007004 EXP DATE 07/2022
lot2110063LOT #2110063 EXP DATE 10/2023 LOT #2007004 EXP DATE 07/2022

Original FDA recall reason

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

Recall details

Recall number
F-0422-2022
Event ID
89000
FDA status
Terminated
Initiated
Nov 9, 2021
Reported
Jan 19, 2022
Classified
Jan 11, 2022
Terminated
May 21, 2024
Quantity
80,169 various bottles and jars
Location
Norcross, GA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

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.

FDA source record · F-0422-2022

Data updated September 16, 2026. View official FDA data ↗

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