Fenugreek Capsules Recalled Due to Foreign Material Contamination
Vitality Works is recalling 100 vegetarian Fenugreek Capsules due to the presence of pen fragments. The affected bottles were distributed to retail customers in the United States.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II recall involving foreign object contamination (pen fragments) in a dietary supplement with no reported illnesses or injuries. Foreign objects present a concrete risk of harm through choking or gastrointestinal injury if consumed, warranting a High severity rating.
Plain-English summary
Vitality Works, Inc. is recalling 100 vegetarian Fenugreek Capsules (90 count, 600mg) due to the presence of foreign material—specifically, pieces of a pen.
The affected product (Lot 2023-06871, expiring 07/2028) was distributed to 55 retail customers representing 284 individual stores throughout the United States. Distribution occurred via parcel shippers, with the distribution chain notified on August 24, 2023. A total of 1,025 bottles were distributed.
Consumers who have purchased this product should discontinue use. For questions about this recall or if you have already consumed the product, contact Vitality Works, Inc.
The recalled product
- Product
- 100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
- Manufacturer
- Vitality Works, Inc
- Category
- Food — Dietary Supplement
- Affected units
- 1,025
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 54 recalled by Vitality Works, Inc 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 54 products in this recall →Related recalls
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