Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 22, 2023 (3 years ago)

vegetarian Fenugreek Capsules recall

Recalled by Vitality Works, Inc · Albuquerque, NM, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Foreign material: pieces of a pen (writing utensil).

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.

Quantity: 1,025 bottles (total)

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 2023-06871 (Lot numbers are generated by our ERP system and use the 4-digit year followed by a 5-digit sequential number.) Expires: 07/2028 Bottom Code: FENUGRK PCAP 202306871 EXP 07/28

Where it was sold

FDA's distribution note: 55 Retail customers, representing 284 individual stores. All customers are located within the United States. There is no foreign distribution. There is no distribution to US Government agencies or departments. Distribution is by small parcel shipper (UPS, FedEx). Distribution Chain Notification Date: August 24, 2023

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Vitality Works, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 22, 2023
In FDA report of
Oct 4, 2023
Terminated
Nov 13, 2023
FDA recall number
F-1582-2023 · event 92936
Official record
FDA enforcement report search

Also recalled with it (53 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Showing 12 of 53.