Vitality Works recalls 100 vegetarian fenugreek capsules (90 count, 600mg) packaged in amber glass with white cap due to foreign material: pen pieces. Consumers should check lot numbers and contact for remedy.
Foreign material: pieces of a pen (writing utensil).
Vitality Works is recalling 100 vegetarian fenugreek capsules (90 count, 600mg) because they contain pieces of a pen. This foreign material could cause choking or injury if swallowed.
The capsules contain pieces of a pen (writing utensil) as foreign material. If swallowed, these pieces could cause choking or injury. The hazard is not severe enough to cause serious injury in normal use.
People who bought the recalled fenugreek capsules from retailers. Those who have the capsules with lot number 2023-06871 or expire by July 2028 are most at risk.
Check for the lot number 2023-06871 on the bottom of the capsule package. The capsules expire by July 2028 and have the code 'FENUGRK PCAP 202306871 EXP 07/28'.
Look for the lot number 2023-06871 on the bottom of the capsule package.
The product contains foreign material (pen pieces) that could cause choking or injury if swallowed, so it is not safe to use.
Check for the lot number 2023-06871 on the bottom of the capsule package. The capsules expire by July 2028 and have the code 'FENUGRK PCAP 202306871 EXP 07/28'.
The recall record does not specify a remedy, so contact Vitality Works for 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-1588-2023 — Vitality Works Vitality Works Hello, I own a Vitality Works that is covered by recall F-1588-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
