BulkSupplements Glucosamine Recall: Undeclared Shellfish Allergen
BulkSupplements.com recalls specific lots of Glucosamine Sulfate Potassium due to undeclared shellfish. Check your lot numbers for safety details.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
Hard Eight Nutrition LLC is recalling BulkSupplements.com Glucosamine Sulfate Potassium because the label failed to declare shellfish as an ingredient. This poses a risk to individuals with shellfish allergies who may unknowingly consume the allergen. The recall affects two specific lots distributed worldwide via the website and Amazon. Read more at govinfonow.com/recall/18759-bulksupplements-glucosamine-recall-undeclared-shellfish-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/18759-bulksupplements-glucosamine-recall-undeclared-shellfish-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-1827-2018
Cite this page
“BulkSupplements Glucosamine Recall: Undeclared Shellfish Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18759-bulksupplements-glucosamine-recall-undeclared-shellfish-allergen. Based on FDA recall #F-1827-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1827-2018%22&limit=1).
Why it’s dangerous
The product label did not list shellfish as an ingredient, although shellfish is properly declared on the website. For people with severe shellfish allergies, ingesting undeclared shellfish can trigger serious allergic reactions.
Who’s affected
Consumers who purchased Glucosamine Sulfate Potassium from BulkSupplements.com or Amazon, particularly those with shellfish allergies. The product was distributed worldwide to countries including Australia, Canada, Germany, Japan, and the United Kingdom.
How to tell if you have this one
Look for BulkSupplements.com Glucosamine Sulfate Potassium in stand-up zipper pouch bags available in 100 grams, 250 grams, 500 grams, or 1 kilogram sizes. Check the package for Lot numbers 121D1214 (Expiration: 12/13/18) or 121E0629 (Expiration: 06/28/19).
- Brand
BulkSupplements- Category
Food
What to do — step by step
Check Your Lot Numbers
Verify if your product matches Lot 121D1214 or Lot 121E0629.
Avoid Consumption If Affected
If you have the recalled lots and have a shellfish allergy, do not consume the product.
How this recall unfolded
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #F-1827-2018 (August 6, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1827-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.