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.
The agency’s classification
FDA (Food): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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
- 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
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.
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