Vitality Works recalls 100 vegetarian fenugreek capsules (90 count, 600mg) due to foreign material: pen pieces. Affected lots include 2023-06871 with expiry 07/2028. Consumers should check packaging for lot number and contact company for remedy.
Foreign material: pieces of a pen (writing utensil).
Vitality Works is recalling 100 vegetarian fenugreek capsules that may contain pieces of a pen. This foreign material could cause choking or injury if swallowed. Consumers should stop using these capsules and contact the company for a replacement.
The capsules may contain small pieces of a pen (writing utensil) that could be swallowed. If ingested, these pieces might cause choking, internal injury, or blockage in the digestive tract.
People who bought the 100 vegetarian fenugreek capsules (90 count, 600mg) with lot number 2023-06871 from Vitality Works. Those who have consumed the capsules are at higher risk of injury from pen pieces.
Check the packaging for the lot number 2023-06871 on the bottom code (FENUGRK PCAP 202306871 EXP 07/28). The capsules are packaged in 150cc amber glass with a white polypropylene cap.
Look for the lot number 2023-06871 on the bottom code of the capsule packaging.
Reach out to Vitality Works for a replacement or refund if you have the affected lot.
The capsules may contain pieces of a pen (writing utensil) that could cause injury if swallowed.
Check the packaging for the lot number 2023-06871 on the bottom code (FENUGRK PCAP 202306871 EXP 07/28).
Yes, you should stop using the capsules and contact Vitality Works for a replacement.
We’ve drafted a message you can send Vitality Works to request your refund or repair — edit it as you like.
Subject: Recall F-1599-2023 — Vitality Works Vitality Works Hello, I own a Vitality Works that is covered by recall F-1599-2023 from Vitality Works. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
