Fenugreek Supplement Capsules Recalled for Pen Pieces Contamination
Vitality Works is recalling 1,025 bottles of 600mg Fenugreek Capsules due to contamination with pen pieces. The affected lot is 2023-06871, expiring July 2028.
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 classified as an FDA Class II recall for foreign material contamination. Although no illnesses or injuries have been reported, the presence of pen pieces in consumed capsules poses a potential choking and injury hazard, meeting the High severity threshold for risk-of-harm products without reported harm.
Plain-English summary
Vitality Works, Inc. is recalling certain Fenugreek Capsules (600mg, 90 count) because pieces of a pen have been found in the product as a contaminant.
The recall affects approximately 1,025 bottles that were distributed to 55 retail customers across 284 individual stores in the United States. No distribution occurred to foreign countries or US Government agencies. The affected lot is 2023-06871, which expires in July 2028.
Consumers who have purchased the recalled product should stop using it immediately and return it to the store where it was purchased. The pen pieces present a potential choking and injury hazard if ingested.
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
- Drug — Dietary Supplement
- Hazard
- 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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