The Recall Desk
SevereFDA (Food)·F-0422-2022·Announced 2022-01-19

CFP Arthro 3000 Capsules Recalled for Undeclared Shellfish

NutraCap Labs is recalling CFP Arthro 3000 Capsules 120ct due to the presence of undeclared shellfish. The product was distributed across 25 states and poses a risk to consumers with shellfish allergies.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: This is an FDA Class I recall for an allergen mislabeling issue. Undeclared shellfish on a food product presents a serious health hazard to allergic consumers and warrants a Severe classification even absent reported illnesses, per the rubric criterion for Class I recalls.

Plain-English summary

NutraCap Labs LLC is recalling CFP (Clark Family Practice) Arthro 3000 Capsules 120ct (UPC 8 60004 06620 0) because the product contains undeclared shellfish. The FDA discovered this issue during an investigation of the firm.

Approximately 80,169 various bottles and jars of the product were distributed to consumers in 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, and WA. The affected product includes LOT #2110063 with expiration date 10/2023 and LOT #2007004 with expiration date 07/2022.

Undeclared shellfish in food products poses a serious health risk to consumers with shellfish allergies, who may experience severe allergic reactions. Consumers who have purchased this product and have a shellfish allergy should stop using it immediately. Anyone who has consumed this product and experienced an allergic reaction should consult a healthcare provider or contact poison control.

The recalled product

Product
CFP (Clark Family Practice) Arthro 3000 Capsules 120ct UPC CODE 8 60004 06620 0
Manufacturer
NutraCap Labs LLC
Category
Food — Dietary Supplements / Nutraceuticals
Hazard
  • allergen-shellfish
  • allergen-mislabeling

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

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

Distribution

Distributed in 26 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

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