The Recall Desk
SevereFDA (Food)·F-0430-2022·Announced 2022-01-19

Dube Ortho & PT capsules recalled for undeclared shellfish

NutraCap Labs LLC is recalling Dube Ortho & PT 144 capsules due to undeclared shellfish in the product. The recall affects 80,169 bottles distributed across 25 states.

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 involving an undeclared major allergen (shellfish) in a dietary supplement. Undeclared allergens present serious risk of anaphylaxis and other allergic reactions in sensitive consumers, even without reported illnesses, meeting the Severe classification threshold.

Plain-English summary

NutraCap Labs LLC is recalling Dube Ortho & PT 144 Bottles Capsules (60 count) because the product contains undeclared shellfish. The FDA discovered this issue during an investigation.

The recalled product was distributed to the following states: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Kentucky, Louisiana, Maryland, Minnesota, North Carolina, New Jersey, Nevada, New York, Ohio, Oregon, South Carolina, Tennessee, Texas, Virginia, and Washington. Affected lots are #2006159 (expiration 06/2022) and #2012121 (expiration 12/2022).

Consumers who have purchased this product and have a shellfish allergy or sensitivity should not consume it. Those with questions about whether their product is affected should contact the manufacturer or consult the recall notice for lot and expiration date information.

The recalled product

Product
Dube Ortho & PT 144 Bottles Capsules 60ct No UPC CODE
Manufacturer
NutraCap Labs LLC
Category
Food — Dietary Supplement
Hazard
Affected units
80,169

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

Distribution

Distributed in 26 states:

Part of a larger recall action

This product is one of 106 recalled by NutraCap Labs LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 106 products in this recall →

Related recalls

Same manufacturer · NutraCap Labs LLC

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Same hazard · allergen shellfish

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