Fenugreek Capsule Supplement Recalled Due to Pen Fragments
Vitality Works is recalling 1,025 bottles of Fenugreek Capsules due to contamination with pieces of a pen. Consumers should stop using the product and return it to the retailer.
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: Foreign material (pen pieces) in an ingestible dietary supplement creates a tangible choking and internal injury risk. FDA Class II classification with no reported illnesses to date meets the criterion of risk-of-harm products where injury has not yet been reported.
Plain-English summary
Vitality Works, Inc. is recalling 1,025 bottles of 100 vegetarian Fenugreek Capsules (90 count, 600mg) due to contamination with foreign material—specifically, pieces of a pen.
The presence of pen fragments in an ingested supplement poses a choking hazard and risk of internal injury if the product is consumed. The contamination was identified during quality control.
The affected product (Lot 2023-06871, expiring 07/2028) was distributed to 55 retail customers representing 284 individual stores across the United States. Distribution chains were notified on August 24, 2023.
Consumers who have this product should stop using it immediately and return it to the point of purchase or discard it. Retailers should remove affected bottles from shelves.
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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