Vitality Works recalls 100 vegetarian fenugreek capsules (90 count, 600mg) due to foreign material: pen pieces. Affected lots include 2023-06871, expiring July 2028. Consumers should check packaging for lot number and contact 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 injury if swallowed. The recall affects specific lots with lot number 2023-06871, expiring July 2028.
The capsules may contain small pieces of a pen (writing utensil) as foreign material. If swallowed, these pieces could cause choking or internal injury. However, the risk is low as the capsules are designed for oral consumption and the foreign material is not a common hazard.
People who purchased the 100 vegetarian fenugreek capsules (90 count, 600mg) with lot number 2023-06871 from Vitality Works. Those who have taken the capsules and are concerned about pen pieces should check their packaging.
Check the packaging for the lot number 2023-06871, which expires July 2028. The product is packaged in 150cc amber glass with a white polypropylene cap. The bottom code on the package reads 'FENUGRK PCAP 202306871 EXP 07/28'.
Look for the lot number 2023-06871 on the packaging, which expires July 2028.
The capsules may contain pieces of a pen (writing utensil) as foreign material.
Check the packaging for the lot number 2023-06871, which expires July 2028. The bottom code reads 'FENUGRK PCAP 202306871 EXP 07/28'.
The recall does not specify a stop-use action, but you should check if you have the recalled lot number and contact Vitality Works for further instructions.
We’ve drafted a message you can send Vitality Works to request your refund or repair — edit it as you like.
Subject: Recall F-1584-2023 — Vitality Works Vitality Works Hello, I own a Vitality Works that is covered by recall F-1584-2023 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.
