The Recall Desk
SevereFDA (Food)·F-0478-2022·Announced 2022-01-19

Rad Jaw Capsules Recalled Due to Undeclared Shellfish

NutraCap Labs LLC is recalling Rad Health Inc. Rad Jaw Capsules (120ct bottles) because the product contains undeclared shellfish, which 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: The FDA classified this as a Class I recall. Although no illnesses or injuries are explicitly reported in the source text, allergen mislabeling of a common allergen (shellfish) in a supplement product presents a serious health risk to affected consumers. Class I classification alone elevates this to at least a severity score of 4 per the rubric.

Plain-English summary

NutraCap Labs LLC is recalling Rad Health Inc. Rad Jaw Capsules in 120-count bottles (UPC 1 95893 50782 5) due to the presence of undeclared shellfish in the product. The recall was initiated after an FDA investigation notified the firm of the undeclared allergen.

The affected 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. A total of 80,169 various bottles and jars are affected.

Consumers who have purchased this product and have a shellfish allergy should stop use immediately. The product may pose a serious health risk to allergic individuals. Consumers with questions or concerns should contact the recalling firm.

Lot numbers affected include #2108321 (expiration 08/2023) and #2105041 (expiration 05/2023).

The recalled product

Product
Rad Health Inc. Rad Jaw Capsules 120ct Bottles UPC CODE 1 95893 50782 5
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 #2108321 EXP DATE 08/2023 LOT #2105041 EXP DATE 05/2023

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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