Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 6, 2018 (8 years ago)

BulkSupplements.com Glucosamine Sulfate Potassium recall

Recalled by Hard Eight Nutrition LLC · Henderson, NV, United States

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

Why it was recalled

FDA inspection found two lots of supplements that did not declare shellfish as an ingredient on the product label; shellfish is properly declared on website.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

BulkSupplements.com Glucosamine Sulfate Potassium; 100 grams, 250 grams, 500 grams, 1 kilogram; Stand up zipper pouch bags. Directions: As a dietary supplement, take 1000 mg (scant 1/4 tsp) up to three time daily, or as directed by a physician. Distributed exclusively by: Bulk Supplements.com 7511 Eastgate Road Henderson, NV 89011

Quantity: 2,100 units

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: 121D1214, Exp: 12/13/18; Lot: 121E0629, Exp: 06/28/19.

Where it was sold

FDA's distribution note: Worldwide sales from website and Amazon. Foreign distribution to: " Australia " Austria " Canada " Czech Republic " Denmark " Finland " France " Germany " Iceland " Isle of Man " Italy " Japan " Liechtenstein " Luxembourg " Netherlands " New Zealand " Norway " South Africa " Sweden " Switzerland " The Philippines " United Kingdom

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
Hard Eight Nutrition LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2018
In FDA report of
Aug 22, 2018
Terminated
Dec 19, 2018
FDA recall number
F-1827-2018 · event 80770
Official record
FDA enforcement report search

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