Fenugreek supplement capsules recalled for pen fragment contamination
Vitality Works is recalling fenugreek supplement capsules (Lot 2023-06871) due to contamination with pen fragments. About 1,025 bottles were distributed to 284 retail store locations across the United States.
What this means for you
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 for foreign material contamination (pen fragments). Per the severity rubric, this qualifies as a risk-of-harm product where injury has not yet been reported, warranting a severity score of 3 (High).
Plain-English summary
Vitality Works, Inc. is recalling its 100 vegetarian fenugreek capsules in Lot 2023-06871 (600mg, 90-count bottles) due to the discovery of foreign material contamination.
The recalled bottles contain fragments of a pen (writing utensil). The affected product has an expiration date of July 2028 and can be identified by the bottom code "FENUGRK PCAP 202306871 EXP 07/28."
Approximately 1,025 bottles were distributed to 55 retail customers representing 284 individual store locations across the United States. The product was distributed via parcel shippers (UPS, FedEx). There is no distribution to foreign countries or U.S. government agencies. Retailers and customers were notified of the recall on August 24, 2023.
Consumers who have purchased this product should stop using it immediately. Those with the affected lot number should discard the product or contact Vitality Works, Inc. for instructions.
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
- 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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