CLASS II Food recall · Reported 22 Aug 2018 · FDA Enforcement Report

BulkSupplements.com Glucosamine Sulfate Potassium;, 1 kilogram recalled

Hard Eight Nutrition is recalling BulkSupplements.com Glucosamine Sulfate Potassium;, 1 kilogram. The recall was initiated on 6 Aug 2018 and the FDA has classified it as Class II.

Check your package

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

Quantity recalled2,100 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1827-2018
FDA event ID: 80770
Recalling firm: Hard Eight Nutrition, Henderson, NV
Brand: BulkSupplements.com Glucosamine
Classification: Class II
Status: Terminated
Recall initiated: 6 Aug 2018
FDA classified: 15 Aug 2018
Reported: 22 Aug 2018
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Fish & Shellfish
Product category: Dietary Supplements

Timeline

6 Aug 2018	Recall initiated by company
15 Aug 2018	Classified by FDA	+9 days
22 Aug 2018	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

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

Where it was distributed

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

Stores named: Amazon, Online Retailers

Questions about this recall

Why was it 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.

Which lots are affected?

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

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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